510(k) Report

510(k) · Cleared

Cleared

Halo Ablation Catheter, Model 90-9100

K093008510(k) TraditionalCleared Jan 8, 2010102-day reviewClass II21 CFR 878.4400

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Barrx Medical, Incorporated · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Jan 8, 2010 as substantially equivalent to K060169 (Barrx Medical, Incorporated, 2006) and 10 other predicates after a 102-day review. Its family tree reaches back 16 generations to 1995. 14 later devices descend from it.

Decided
Jan 8, 2010
Review
102 days
Class
Class II
Product code
GEI
Recalls
None
Predicates
11

Its longest line of descent runs back 16 generations to K943450 (1995). 39 ancestors in all, the oldest K800617 (1980). 14 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2006: 1 other ancestor2005: 1 other ancestor1998: 3 other ancestors1997: 1 other ancestor2007: 1 other ancestor2002: 1 other ancestor2000: 1 other ancestor1996: 5 other ancestors1994: 1 other ancestor1985: 2 other ancestors1984: 1 other ancestor1992: 1 other ancestor1986: 1 other ancestor1980: 1 other ancestor1995: 1 other ancestor2012: 2 descendants cleared2014: 1 descendant cleared2019: 1 descendant cleared2013: 1 descendant cleared2010: 1 descendant cleared2015: 1 descendant cleared2017: 1 descendant cleared2018: 1 descendant cleared2016: 1 descendant cleared2024: 1 descendant cleared2021: 2 descendants cleared2025: 1 descendant clearedK943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995×2: 2 generations cleared close together, K961069 (1996), K962445 (1996) ×2: 2 generations cleared close together, K964849 (1997), K971532 (1997) K013139 · Stellartech Coagulation System · Stellartech Research Corp. · 2001×3: 3 generations cleared close together, K032062 (2003), K032452 (2003), K032721 (2003) ×4: 4 generations cleared close together, K040240 (2004), K041383 (2004), K042909 (2004), K050831 (2005) K060169 · Barrx Halo Coagulation System, Barrx Halo Coagulation Generator, Barrx Coagulation Catheter, Models 2200-115A, 1520F · Barrx Medical, Incorporated · 2006K062723 · HALO90 Coagulation Catheter · Barrx Medical, Incorporated · 2006K083711 · Modification to: Halo Coagulation Catheter, Models 32041-18, 32041-20, 32041-22, 32041-25, 32041-28, 32041-31, 32041-34 · Barrx Medical, Incorporated · 200919801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 5 other ancestors2 generations back: 9 other ancestors3 generations back: 6 other ancestors4 generations back: 3 other ancestors 1 generation forward: 5 descendants2 generations forward: 9 descendants K083711 · Modification to: Halo Coagulation Catheter, Models 32041-18, 32041-20, 32041-22, 32041-25, 32041-28, 32041-31, 32041-34 · Barrx Medical, Incorporated · 2009K062723 · HALO90 Coagulation Catheter · Barrx Medical, Incorporated · 2006K060169 · Barrx Halo Coagulation System, Barrx Halo Coagulation Generator, Barrx Coagulation Catheter, Models 2200-115A, 1520F · Barrx Medical, Incorporated · 2006K050831 · Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230A · Stellartech Research Corp. · 2005K042909 · Stellartech Coagulation System, Models 1100C-115A & 1100C-230A · Stellartech Research Corp. · 2004K041383 · Stellartech Coagulation System, Models 1100C-115 and 1100C-230 · Stellartech Research Corp. · 2004K040240 · Stellartech Coagulation System (Models 1100C-115 & 1100C-230) · Stellartech Research Corp. · 2004K032721 · Modification to: Stellartech Coagulation System (Models 1100C-115 & 1100C-230) · Stellartech Research Corp. · 2003K032452 · Modification to: Stellartech Coagulation System, Models 1100C-115 & 100C-230 · Stellartech Research Corp. · 2003K032062 · Stellartech Coagulation System, Models (1100C-115 & 1100C-230) · Stellartech Research Corp. · 2003K013139 · Stellartech Coagulation System · Stellartech Research Corp. · 2001K971532 · Arthrocare Electrosurgery System · Arthrocare Corp. · 1997K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K962445 · Arthrocare Dental Electrosurgery System · Arthrocare Corp. · 1996K961069 · Arthrocare Urologic Multi-Electrode Electrosurgery System · Arthrocare Corp. · 1996K943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995−15−10−50
  1. Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 12 generations between
  3. 3 generations backK060169 Barrx Halo Coagulation System, Barrx Halo Coagulation Generator…Barrx Medical, Incorporated · 2006
  4. 2 generations backK062723 HALO90 Coagulation CatheterBarrx Medical, Incorporated · 2006
  5. 1 generation backK083711 Modification to: Halo Coagulation Catheter, Models 32041-18…Barrx Medical, Incorporated · 2009
  6. This deviceK093008 Halo Ablation Catheter, Model 90-9100Barrx Medical, Incorporated · 2010
  7. Descendant · cites it directly · 4 of its ownK183595 Aqua Medical RF Vapor SystemAqua Medical, Inc. · 2019
  8. Descendant · cites it directly · 4 of its ownK112454 HALO60 Ablation CatheterBarrx Medical, Inc. · 2012
  9. Descendant · 2 generations on · 3 of its ownK211282 Aqua Medical RF Vapor SystemAqua Medical, Inc. · 2021
  10. Descendant · 2 generations on · 2 of its ownK213627 RF Vapor SystemAqua Medical, Inc. · 2021
  11. Descendant · 2 generations on · 1 of its ownK241271 Aqua Medical RF Vapor Ablation SystemAqua Medical, Inc. · 2024
Show all 16 generations
  1. Root · 16 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 15 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 14 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 13 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 12 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
  6. 11 generations backK013139 Stellartech Coagulation SystemStellartech Research Corp. · 2001
  7. 10 generations backK032062 Stellartech Coagulation System, Models (1100C-115 & 1100C-230)Stellartech Research Corp. · 2003
  8. 9 generations backK032452 Modification to: Stellartech Coagulation System, Models 1100C-115 &…Stellartech Research Corp. · 2003
  9. 8 generations backK032721 Modification to: Stellartech Coagulation System (Models 1100C-115 &…Stellartech Research Corp. · 2003
  10. 7 generations backK040240 Stellartech Coagulation System (Models 1100C-115 & 1100C-230)Stellartech Research Corp. · 2004
  11. 6 generations backK041383 Stellartech Coagulation System, Models 1100C-115 and 1100C-230Stellartech Research Corp. · 2004
  12. 5 generations backK042909 Stellartech Coagulation System, Models 1100C-115A & 1100C-230AStellartech Research Corp. · 2004
  13. 4 generations backK050831 Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230AStellartech Research Corp. · 2005
  14. 3 generations backK060169 Barrx Halo Coagulation System, Barrx Halo Coagulation Generator…Barrx Medical, Incorporated · 2006
  15. 2 generations backK062723 HALO90 Coagulation CatheterBarrx Medical, Incorporated · 2006
  16. 1 generation backK083711 Modification to: Halo Coagulation Catheter, Models 32041-18…Barrx Medical, Incorporated · 2009
  17. This deviceK093008 Halo Ablation Catheter, Model 90-9100Barrx Medical, Incorporated · 2010

Showing 5 of 14 descendants. See all descendants

Descendants cleared per year

2010: 12012: 22013: 12014: 12015: 12016: 12017: 12018: 12019: 12021: 22024: 12025: 1
2010high 2 (2012) · low 0 (2011)2026

Most influential descendants

Showing 5 of 14 · See all
  • K183595Aqua Medical RF Vapor SystemAqua Medical, Inc. · 2019 · cites it directly4descendants
  • K112454HALO60 Ablation CatheterBarrx Medical, Inc. · 2012 · cites it directly4descendants
  • K211282Aqua Medical RF Vapor SystemAqua Medical, Inc. · 2021 · 2 generations on3descendants
  • K213627RF Vapor SystemAqua Medical, Inc. · 2021 · 2 generations on2descendants
  • K241271Aqua Medical RF Vapor Ablation SystemAqua Medical, Inc. · 2024 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−16K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−15K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−14K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−13K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−12K971532Arthrocare Electrosurgery SystemArthrocare Corp.1997—
−11K013139Stellartech Coagulation SystemStellartech Research Corp.2001—
−10K032062Stellartech Coagulation System, Models (1100C-115 & 1100C-230)Stellartech Research Corp.2003—
−9K032452Modification to: Stellartech Coagulation System, Models 1100C-115 & 100C-230Stellartech Research Corp.2003—
−8K032721Modification to: Stellartech Coagulation System (Models 1100C-115 & 1100C-230)Stellartech Research Corp.2003—
−7K040240Stellartech Coagulation System (Models 1100C-115 & 1100C-230)Stellartech Research Corp.2004—
−6K041383Stellartech Coagulation System, Models 1100C-115 and 1100C-230Stellartech Research Corp.2004—
−5K042909Stellartech Coagulation System, Models 1100C-115A & 1100C-230AStellartech Research Corp.2004—
−4K050831Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230AStellartech Research Corp.2005—
−3K060169Barrx Halo Coagulation System, Barrx Halo Coagulation Generator, Barrx…Barrx Medical, Incorporated2006—
−2K062723HALO90 Coagulation CatheterBarrx Medical, Incorporated2006—
−1K083711Modification to: Halo Coagulation Catheter, Models 32041-18, 32041-20…Barrx Medical, Incorporated2009—
0 (this device)K093008Halo Ablation Catheter, Model 90-9100Barrx Medical, Incorporated2010—
+1K183595Aqua Medical RF Vapor SystemAqua Medical, Inc.2019—
+1K112454HALO60 Ablation CatheterBarrx Medical, Inc.2012—
+2K211282Aqua Medical RF Vapor SystemAqua Medical, Inc.2021—
+2K213627RF Vapor SystemAqua Medical, Inc.2021—
+2K241271Aqua Medical RF Vapor Ablation SystemAqua Medical, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198410
198520
198610
199210
199410
199510
199650
199710
199830
200010
200210
200510
200610
200710
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201220
201310
201410
201510
201610
201710
201810
201910
202120
202410
202510
FIG. 1 — Lineage of K093008, 1995–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GEI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new GEI device

  1. #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (11)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K060169Barrx Halo Coagulation System, Barrx Halo Coagulation Generator, Barrx Coagulation…
Summary page 1
…Name Electrosurgical Coagulation System Classification Name Electrosurgical Cutting or Coagulation Device Predicate Devices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909…
Barrx Medical, Incorporated2006—
*K062723HALO90 Coagulation Catheter
Summary page 1
…rosurgical Coagulation System Classification Name Electrosurgical Cutting or Coagulation Device Predicate Devices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831…
Barrx Medical, Incorporated2006—
*K083737Halo Ablation Catheter
Summary page 1
…oagulation System Classification Name Electrosurgical Cutting or Coagulation Device Predicate Devices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasiv…
Barrx Medical, Incorporated2009—
*K051168Barrx Halo 360 System, Model 1100C-115A
Our reading of the summary gave K050168, FDA’s number for Langston Dual Lumen Pressure Monitoring Catheter (Vascular Solutions, Inc.). Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “HALO 360 Ablation Catheter”.
Barrx Medical, Incorporated2005—
*K062225Halo Coagulation Catheter
Summary page 1
…surgical Cutting or Coagulation Device Predicate Devices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982…
Barrx Medical, Incorporated2006—
*K083711Modification to: Halo Coagulation Catheter, Models 32041-18, 32041-20, 32041-22…
Summary page 1
…Cutting or Coagulation Device Predicate Devices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Inte…
Barrx Medical, Incorporated2009—
*K013139Stellartech Coagulation System
Summary page 1
…vices HALO 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Intended Use!/ Indications for Use…
Stellartech Research Corp.2001—
*K042909Stellartech Coagulation System, Models 1100C-115A & 1100C-230A
Summary page 1
…O 90 Ablation Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Intended Use!/ Indications for Use…
Stellartech Research Corp.2004—
*K050831Stellartech Coagulation System 2, Models 1100C-115A and 1100C-230A
Summary page 1
…tion Catheter model 90-91100 (K060 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Intended Use!/ Indications for Use…
Stellartech Research Corp.2005—
*K970278Microvasive Gold Probe
Summary page 1
…0 169, K062723 and K083737) HALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Intended Use!/ Indications for Use 9 Ablation Cathete…
Boston Scientific Corp1997—
*K982289Heat Probe Unit Hpu-20, Heat Probe CD-110##/120##
Summary page 1
…ALO 360 Ablation Catheter (KO5O0168, K062225, K08371 1) Stellartech Coagulation Catheter (K013139, K042909, K050831) Microvasive Gold Probe (K970278) Olympus Heat Probe (K982289) Intended Use!/ Indications for Use 9 Ablation Catheter model 90-9 100 and T…
Olympus America, Inc.1998—

Also cleared against K060169: 5 other devices →

What descends from it? (14)

See all 14

5 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K183595Aqua Medical RF Vapor SystemAqua Medical, Inc.20194
K112454HALO60 Ablation CatheterBarrx Medical, Inc.20124
K141357Barrx Flex Rfa Energy GeneratorCovidien Iic20141
K130623Barrx Channel Rfa Endoscopic CatheterCovidien, LLC20131
K101111Halo Ablation Catheter Model 90-9100, HALO90 Ultra Ablation Catheter Model 90-9200Barrx Medical, Inc.20101

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 15 years and passes through 3 companies; a new generation was cleared every 7 months on median.
  • 1 of the 39 ancestors has a recall of any class.
  • Of its descendants, K183595 (Aqua Medical, Inc., 2019) has gone furthest, with 4 descendants of its own.
  • 5 other devices also cite its predicate K060169.

How does its category compare?

All GEI devices

GEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · GEI

52in 2025

2007: 502008: 612009: 422010: 462011: 352012: 392013: 482014: 492015: 472016: 642017: 522018: 472019: 482020: 592021: 462022: 552023: 652024: 592025: 522026 (partial year): 43
2007high 65 (2023) · low 35 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEI

113in 2025

2007: 51 days median2008: 71 days median2009: 130 days median2010: 109 days median2011: 135 days median2012: 133 days median2013: 136 days median2014: 103 days median2015: 123 days median2016: 108 days median2017: 72 days median2018: 93 days median2019: 93 days median2020: 105 days median2021: 146 days median2022: 150 days median2023: 104 days median2024: 125 days median2025: 113 days median2026 (partial year): 183 days median
2007high 183 (2026) · low 51 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GEI

4in 2025

2007: 212008: 192009: 272010: 512011: 322012: 302013: 132014: 32015: 42016: 32017: 22018: 62019: 52020: 12021: 62022: 492023: 27, 4 Class I2024: 22, 10 Class I2025: 42026 (partial year): 8
2007high 51 (2010) · low 1 (2020)2026

Class I (14 since 2007) Class II/III not classified

Adverse event reports per year · GEI

7,592in 2025

2007: 2,7952008: 2,5562009: 3,5912010: 3,3772011: 4,4632012: 5,2162013: 4,8972014: 4,9082015: 4,9362016: 5,6162017: 6,0732018: 6,5452019: 7,0672020: 6,4902021: 6,3542022: 6,1032023: 7,1762024: 7,8972025: 7,592
2007high 7,897 (2024) · low 2,556 (2008)2025

MAUDE reports naming product code GEI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20075051212,795
20086171192,556
200942130273,591
201046109513,377
201135135324,463
201239133305,216
201348136134,897
20144910334,908
20154712344,936
20166410835,616
2017527226,073
2018479366,545
2019489357,067
20205910516,490
20214614666,354
202255150496,103
20236510427 (4)7,176
20245912522 (10)7,897
20255211347,592
2026431838—

What is it indicated for?

The HALO 90 System (including HALO 90 Ablation Catheter model 90-9100 and HALO 90 Energy Generator model 90-9000) is indicated for use in the coagulation of bleeding and non-bleeding sites in the gastrointestinal tract including but not limited to the esophagus.

Indications include Esophageal Ulcers, Mallory-Weiss tears, Arteriovenous Malformations, Angiomata, Barrett's Esophagus, Dieulafoy Lesions, Angiodysplasia, Gastric Antral Vascular Ectasia (GAVE) and Radiation Proctitis (RP).

Indications for use as stated in the FDA summary.

Also cleared against K060169

5 other devices cite the same predicate.

  • K183595Aqua Medical RF Vapor SystemAqua Medical, Inc. · 2019
  • K101111Halo Ablation Catheter Model 90-9100, HALO90 Ultra Ablation Catheter Model 90-9200Barrx Medical, Inc. · 20101 recall
  • K092487Haloflex Energy Generator, Models 1190A-115A and 1190A-230ABarrx Medical, Incorporated · 20091 recall
  • K062441Barrx Halo Coagulation System; Generator, Model 90-9000; Output Cable, Model 90-9010; Footswitch, Model…Barrx Medical, Incorporated · 2006
  • K062723HALO90 Coagulation CatheterBarrx Medical, Incorporated · 2006

More from Barrx Medical, Incorporated

13 FDA decisions under this applicant name. See the company

  • K093855Halo 360 & Sizing Balloon, Model 3441CBarrx Medical, Incorporated · 2010
  • K092487Haloflex Energy Generator, Models 1190A-115A and 1190A-230ABarrx Medical, Incorporated · 20091 recall
  • K083737Halo Ablation CatheterBarrx Medical, Incorporated · 2009
  • K083711Modification to: Halo Coagulation Catheter, Models 32041-18, 32041-20, 32041-22, 32041-25, 32041-28…Barrx Medical, Incorporated · 2009
  • K082202HALO360 Energy Generator, Models 1100C-115B and 1100C-230BBarrx Medical, Incorporated · 2008

Recent decisions in GEI

The GEI category page

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https://510kreport.com/device/K093008 · printed Nov 5, 2026

Cite this page

510(k) Report. “K093008: Halo Ablation Catheter, Model 90-9100.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K093008

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026