510(k) Report

510(k) · Cleared

Cleared

swiftPro System

K222388510(k) TraditionalCleared May 4, 2023269-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

Emblation, Ltd. · NEY System, Ablation, Microwave And Accessories

Cleared on May 4, 2023 as substantially equivalent to K181941 (Emblation, Ltd., 2018) after a 269-day review. Its family tree reaches back 11 generations to 1987. 2 later devices descend from it.

Decided
May 4, 2023
Review
269 days
Class
Class II
Product code
NEY
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K870028 (1987). 56 ancestors in all, the oldest K790187 (1979). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2008: 1 other ancestor2006: 3 other ancestors2002: 5 other ancestors2001: 3 other ancestors1999: 3 other ancestors2003: 6 other ancestors1998: 3 other ancestors1996: 3 other ancestors1986: 2 other ancestors2007: 1 other ancestor2000: 2 other ancestors1984: 2 other ancestors1983: 1 other ancestor1997: 4 other ancestors1979: 1 other ancestor1988: 1 other ancestor1981: 1 other ancestor1995: 1 other ancestor1991: 1 other ancestor2024: 1 descendant cleared2025: 1 descendant clearedK870028 · SMK Sluyter-Mehta Cannulae, RF Pole, Pole,Flexible · Radionics, Inc. · 1987K963577 · Radionics Sluijter-Mehta Cannula · Radionics, Inc. · 1996K980430 · Radionics Disposable RF Cannulae (SC-C, RFK-DB, RFK-DS) · Radionics, Inc. · 1998K021329 · Rita System · Rita Medical Systems · 2002K042216 · Cool-Tip RF Ablation System · Valleylab · 2004K053290 · Cool-Tip RF Generator, Cool-Tip RF System Accessories · Valleylab · 2006K072687 · Valleylab Microwave Ablation Generator · Covidien Lp, Formerly Know AS Valleylab, A Divison · 2008K100744 · Certus 140 Microwave Ablation System and Accessories, Model Certus 140 · Neuwave Medical, Inc. · 2010K113237 · Certus 140 2.45GHZ Ablation System · Neuwave Medical, Inc. · 2012K133821 · Emprint Ablation System · Covidien, LLC · 2014 · recalledK181941 · Swift System · Emblation, Ltd. · 201819801990200020102020
  1. Root · 11 generations backK870028 SMK Sluyter-Mehta Cannulae, RF Pole, Pole,FlexibleRadionics, Inc. · 1987
  2. 7 generations between
  3. 3 generations backK113237 Certus 140 2.45GHZ Ablation SystemNeuwave Medical, Inc. · 2012
  4. 2 generations backK133821 Emprint Ablation SystemCovidien, LLC · 2014 · Recalled
  5. 1 generation backK181941 Swift SystemEmblation, Ltd. · 2018
  6. This deviceK222388 swiftPro SystemEmblation, Ltd. · 2023
  7. Descendant · cites it directly · 1 of its ownK240518 swiftPro™ SystemEmblation Limited · 2024
  8. Descendant · 2 generations on · 0 of its ownK250718 swiftPro System (SWF-SPS); Swift System (SWF-SYS)Emblation Limited · 2025
Show all 11 generations
  1. Root · 11 generations backK870028 SMK Sluyter-Mehta Cannulae, RF Pole, Pole,FlexibleRadionics, Inc. · 1987
  2. 10 generations backK963577 Radionics Sluijter-Mehta CannulaRadionics, Inc. · 1996
  3. 9 generations backK980430 Radionics Disposable RF Cannulae (SC-C, RFK-DB, RFK-DS)Radionics, Inc. · 1998
  4. 8 generations backK021329 Rita SystemRita Medical Systems · 2002
  5. 7 generations backK042216 Cool-Tip RF Ablation SystemValleylab · 2004
  6. 6 generations backK053290 Cool-Tip RF Generator, Cool-Tip RF System AccessoriesValleylab · 2006
  7. 5 generations backK072687 Valleylab Microwave Ablation GeneratorCovidien Lp, Formerly Know AS Valleylab, A Divison · 2008
  8. 4 generations backK100744 Certus 140 Microwave Ablation System and Accessories, Model Certus 140Neuwave Medical, Inc. · 2010
  9. 3 generations backK113237 Certus 140 2.45GHZ Ablation SystemNeuwave Medical, Inc. · 2012
  10. 2 generations backK133821 Emprint Ablation SystemCovidien, LLC · 2014 · Recalled
  11. 1 generation backK181941 Swift SystemEmblation, Ltd. · 2018
  12. This deviceK222388 swiftPro SystemEmblation, Ltd. · 2023

Most influential descendants

Showing 2 of 2 · See all
  • K240518swiftPro™ SystemEmblation Limited · 2024 · cites it directly1descendant
  • K250718swiftPro System (SWF-SPS); Swift System (SWF-SYS)Emblation Limited · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K870028SMK Sluyter-Mehta Cannulae, RF Pole, Pole,FlexibleRadionics, Inc.1987—
−10K963577Radionics Sluijter-Mehta CannulaRadionics, Inc.1996—
−9K980430Radionics Disposable RF Cannulae (SC-C, RFK-DB, RFK-DS)Radionics, Inc.1998—
−8K021329Rita SystemRita Medical Systems2002—
−7K042216Cool-Tip RF Ablation SystemValleylab2004—
−6K053290Cool-Tip RF Generator, Cool-Tip RF System AccessoriesValleylab2006—
−5K072687Valleylab Microwave Ablation GeneratorCovidien Lp, Formerly Know AS Valleylab, A Divison2008—
−4K100744Certus 140 Microwave Ablation System and Accessories, Model Certus 140Neuwave Medical, Inc.2010—
−3K113237Certus 140 2.45GHZ Ablation SystemNeuwave Medical, Inc.2012—
−2K133821Emprint Ablation SystemCovidien, LLC20147
−1K181941Swift SystemEmblation, Ltd.2018—
0 (this device)K222388swiftPro SystemEmblation, Ltd.2023—
+1K240518swiftPro™ SystemEmblation Limited2024—
+2K250718swiftPro System (SWF-SPS); Swift System (SWF-SYS)Emblation Limited2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198110
198310
198420
198620
198810
199110
199510
199630
199740
199830
199930
200020
200130
200250
200360
200630
200710
200810
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202510
FIG. 1 — Lineage of K222388, 1987–2025Source: 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 NEY? 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 NEY device

  1. #1 K253771 Disposable Microwave Ablation Antenna…score 14.5 · 13 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? (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
*K181941Swift System
Summary page 4
…NEY III. PREDICATE DEVICE Trade Name: Swift® System Common Name: Microwave ablation system and accessories 510(k) Number K181941 Manufacturer: Emblation Limited Regulatory Class II Product Code: NEY This predicate has not…
Emblation, Ltd.2018—

Also cleared against K181941: 1 other device →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K240518swiftPro™ SystemEmblation Limited20241

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 36 years and passes through 7 companies; a new generation was cleared every 2.3 years on median.
  • 8 of the 56 ancestors have a recall of any class.
  • Of its descendants, K240518 (Emblation Limited, 2024) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K181941.

How does its category compare?

All NEY devices

NEY System, Ablation, Microwave And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · NEY

1in 2025

2007: 22008: 32009: 42010: 32012: 32013: 12014: 12015: 22016: 32017: 32018: 32019: 22020: 72021: 42022: 12023: 92024: 72025: 12026 (partial year): 2
2007high 9 (2023) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NEY

94in 2024

2008: 145 days median2009: 169 days median2010: 219 days median2012: 81 days median2016: 30 days median2017: 121 days median2018: 90 days median2020: 178 days median2021: 379 days median2023: 155 days median2024: 94 days median
2007high 379 (2021) · low 30 (2016)2026

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

Recalls per year · NEY

1in 2022

2017: 122018: 32021: 12022: 1
2007high 12 (2017) · low 0 (2007)2026

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

Adverse event reports per year · NEY

112in 2025

2007: 182008: 152009: 72010: 282011: 262012: 92013: 162014: 272015: 922016: 1762017: 2252018: 1022019: 1232020: 1282021: 2172022: 1422023: 1062024: 1412025: 112
2007high 225 (2017) · low 7 (2009)2025

MAUDE reports naming product code NEY, 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
20072—018
20083145015
2009416907
20103219028
20110—026
201238109
20131—016
20141—027
20152—092
20163300176
2017312112225
20183903102
20192—0123
202071780128
202143791217
20221—1142
202391550106
20247940141
20251—0112
20262—0—

What is it indicated for?

The swiftPro™ System is a surface based device intended for the coagulation of soft tissue during non-invasive procedures.

The swiftPro™ System is not indicated for use in cardiac procedures.

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. “K222388: swiftPro System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K222388

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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