510(k) Report

510(k) · Cleared

Cleared

Vortex Radial Spray Catheter

K201183510(k) TraditionalCleared Dec 7, 2020220-day reviewClass II21 CFR 878.4350

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

CSA Medical, Inc. · GEH Unit, Cryosurgical, Accessories

Cleared on Dec 7, 2020 as substantially equivalent to K171626 (CSA Medical, Inc., 2017) after a 220-day review. Its family tree reaches back 17 generations to 2001.

Decided
Dec 7, 2020
Review
220 days
Class
Class II
Product code
GEH
Recalls
None
Predicates
1

Its longest line of descent runs back 17 generations to K003811 (2001). 29 ancestors in all, the oldest K790187 (1979). No later device cites it as a predicate yet.

Other ancestors, by generation 10 generations back: 2 other ancestors11 generations back: 4 other ancestors12 generations back: 2 other ancestors13 generations back: 1 other ancestor14 generations back: 3 other ancestors K171626 · truFreeze System · CSA Medical, Inc. · 2017K163244 · truFreeze System · CSA Medical, Inc. · 2017K162695 · truFreeze System · CSA Medical, Inc. · 2016K161557 · truFreeze System · CSA Medical, Inc. · 2016K160273 · truFreeze System · Csa Medial, Inc. · 2016K152668 · truFreeze System · CSA Medical, Inc. · 2015K150920 · truFreeze System · CSA Medical, Inc. · 2015K143625 · truFreeze System · CSA Medical, Inc. · 2015 · recalledK133258 · Trufreeze System · CSA Medical, Inc. · 2014 · recalledK102360 · Icesence 3 · IceCure Medical, Ltd. · 2010 · recalledK062896 · V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models; VS3000, VP0600, VD0600 · Sanarus Medical, Inc. · 2007K061510 · Sanarus Visica Treatment System · Sanarus Medical, Inc. · 2006K052861 · Modification to:Sanarus Visica Treatment System , Models VS2000 · Sanarus Medical, Inc. · 2005K022314 · Sanarus Visica Treatment System · Sanarus Medical, Inc. · 2002 · recalledK021211 · Modification to Sanarus Visica Treatment System · Sanarus Medical, Inc. · 2002K020605 · Sanarus Visica Treatment System · Sanarus Medical, Inc. · 2002K003811 · Cryocare Surgical System · Endocare, Inc. · 2001−15−10−50
  1. Root · 17 generations backK003811 Cryocare Surgical SystemEndocare, Inc. · 2001
  2. 13 generations between
  3. 3 generations backK162695 truFreeze SystemCSA Medical, Inc. · 2016
  4. 2 generations backK163244 truFreeze SystemCSA Medical, Inc. · 2017
  5. 1 generation backK171626 truFreeze SystemCSA Medical, Inc. · 2017
  6. This deviceK201183 Vortex Radial Spray CatheterCSA Medical, Inc. · 2020
Show all 17 generations
  1. Root · 17 generations backK003811 Cryocare Surgical SystemEndocare, Inc. · 2001
  2. 16 generations backK020605 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002
  3. 15 generations backK021211 Modification to Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002
  4. 14 generations backK022314 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2002 · Recalled
  5. 13 generations backK052861 Modification to:Sanarus Visica Treatment System , Models VS2000Sanarus Medical, Inc. · 2005
  6. 12 generations backK061510 Sanarus Visica Treatment SystemSanarus Medical, Inc. · 2006
  7. 11 generations backK062896 V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models…Sanarus Medical, Inc. · 2007
  8. 10 generations backK102360 Icesence 3IceCure Medical, Ltd. · 2010 · Recalled
  9. 9 generations backK133258 Trufreeze SystemCSA Medical, Inc. · 2014 · Recalled
  10. 8 generations backK143625 truFreeze SystemCSA Medical, Inc. · 2015 · Recalled
  11. 7 generations backK150920 truFreeze SystemCSA Medical, Inc. · 2015
  12. 6 generations backK152668 truFreeze SystemCSA Medical, Inc. · 2015
  13. 5 generations backK160273 truFreeze SystemCsa Medial, Inc. · 2016
  14. 4 generations backK161557 truFreeze SystemCSA Medical, Inc. · 2016
  15. 3 generations backK162695 truFreeze SystemCSA Medical, Inc. · 2016
  16. 2 generations backK163244 truFreeze SystemCSA Medical, Inc. · 2017
  17. 1 generation backK171626 truFreeze SystemCSA Medical, Inc. · 2017
  18. This deviceK201183 Vortex Radial Spray CatheterCSA Medical, Inc. · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−17K003811Cryocare Surgical SystemEndocare, Inc.2001—
−16K020605Sanarus Visica Treatment SystemSanarus Medical, Inc.2002—
−15K021211Modification to Sanarus Visica Treatment SystemSanarus Medical, Inc.2002—
−14K022314Sanarus Visica Treatment SystemSanarus Medical, Inc.20021
−13K052861Modification to:Sanarus Visica Treatment System , Models VS2000Sanarus Medical, Inc.2005—
−12K061510Sanarus Visica Treatment SystemSanarus Medical, Inc.2006—
−11K062896V2 Treatment System (V2 Console, V2 Ice Probe, V2 Dewars) Models; VS3000…Sanarus Medical, Inc.2007—
−10K102360Icesence 3IceCure Medical, Ltd.20101
−9K133258Trufreeze SystemCSA Medical, Inc.20141
−8K143625truFreeze SystemCSA Medical, Inc.20151
−7K150920truFreeze SystemCSA Medical, Inc.2015—
−6K152668truFreeze SystemCSA Medical, Inc.2015—
−5K160273truFreeze SystemCsa Medial, Inc.2016—
−4K161557truFreeze SystemCSA Medical, Inc.2016—
−3K162695truFreeze SystemCSA Medical, Inc.2016—
−2K163244truFreeze SystemCSA Medical, Inc.2017—
−1K171626truFreeze SystemCSA Medical, Inc.2017—
0 (this device)K201183Vortex Radial Spray CatheterCSA Medical, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198410
199010
199510
199740
199810
200110
200510
200710
FIG. 1 — Lineage of K201183, 2001–2020Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 GEH? 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 GEH device

  1. #1 K211099 Freeze’n Clear Skin Clinic Warts & Tagsscore 25.4 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K171626truFreeze System
Summary page 4
…21 CFR 878.4350 Product Code: GEH Device Classification: Class II Predicate Device truFreeze System, K171626 1…
CSA Medical, Inc.2017—

Also cleared against K171626: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 19 years and passes through 5 companies; a new generation was cleared every 5 months on median.
  • 4 of the 29 ancestors have a recall of any class.
  • 1 other device also cites its predicate K171626.

How does its category compare?

All GEH devices

GEH Unit, Cryosurgical, Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · GEH

10in 2025

2007: 62008: 12009: 42010: 42011: 72012: 42013: 42014: 62015: 112016: 152017: 122018: 62019: 62020: 82021: 62022: 62023: 82024: 92025: 102026 (partial year): 8
2007high 15 (2016) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEH

77in 2025

2007: 71 days median2009: 121 days median2010: 86 days median2011: 91 days median2012: 96 days median2013: 76 days median2014: 42 days median2015: 72 days median2016: 60 days median2017: 83 days median2018: 42 days median2019: 115 days median2020: 113 days median2021: 206 days median2022: 56 days median2023: 136 days median2024: 85 days median2025: 77 days median2026 (partial year): 148 days median
2007high 206 (2021) · low 42 (2014)2026

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

Recalls per year · GEH

2in 2023

2007: 32008: 22009: 132010: 42012: 32014: 22018: 12019: 12020: 372023: 22026 (partial year): 2
2007high 37 (2020) · low 0 (2011)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GEH

171in 2025

2007: 232008: 292009: 212010: 1732011: 612012: 912013: 912014: 572015: 972016: 1432017: 2162018: 2082019: 4552020: 2772021: 2132022: 2302023: 1642024: 1412025: 171
2007high 455 (2019) · low 21 (2009)2025

MAUDE reports naming product code GEH, 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
2007671323
20081—229
200941211321
20104864173
2011791061
2012496391
2013476091
2014642257
20151172097
201615600143
201712830216
20186421208
201961151455
2020811337277
202162060213
20226560230
202381362164
20249850141
202510770171
202681482—

What is it indicated for?

Intended Use:

The truFreeze® System is intended for cryogenic destruction of tissue using Liquid Nitrogen spray that has a boiling point of -196°C, requiring either active or passive venting during surgical procedures.

Indications for Use, Vortex™ Radial Spray catheter:

The Vortex™ Radial Spray catheter is indicated for use as a cryosurgical tool to ablate benign (e.g., Barrett's Esophagus with high grade and/or low grade dysplasia) in the upper gastrointestinal tract using active venting.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K201183: Vortex Radial Spray Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201183

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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