510(k) Report

510(k) · Cleared

Cleared

Selector Ultrasonic Surgical Aspirator

K901974510(k) TraditionalCleared Sep 5, 1990127-day reviewClass U

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

Spembly Medical, Ltd. · LFL Instrument, Ultrasonic Surgical

Cleared on Sep 5, 1990 after a 127-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 18 later devices descend from it.

Decided
Sep 5, 1990
Review
127 days
Class
Class U
Product code
LFL
Recalls
None
Predicates
0

18 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2008: 1 descendant cleared2011: 2 descendants cleared2009: 1 descendant cleared2016: 1 descendant cleared2012: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant cleared2024: 1 descendant cleared2025: 1 descendant cleared2019: 1 descendant cleared2023: 2 descendants cleared2022: 3 descendants cleared2026: 1 descendant cleared1990200020102020
  1. This deviceK901974 Selector Ultrasonic Surgical AspiratorSpembly Medical, Ltd. · 1990
  2. Descendant · cites it directly · 17 of its ownK042277 Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd. · 2004
  3. Descendant · 2 generations on · 16 of its ownK081459 Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc. · 2008 · Recalled
  4. Descendant · 3 generations on · 11 of its ownK161882 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2016 · Recalled
  5. Descendant · 4 generations on · 10 of its ownK182809 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2018 · Recalled
  6. Descendant · 5 generations on · 5 of its ownK200774 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2020

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

2004: 12008: 12009: 12011: 22012: 12016: 12018: 12019: 12020: 12022: 32023: 22024: 12025: 12026: 1
2004high 3 (2022) · low 0 (2005)2026

Most influential descendants

Showing 5 of 18 · See all
  • K042277Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd. · 2004 · cites it directly17descendants
  • K081459Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc. · 2008 · 2 generations on16descendants
  • K161882CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2016 · 3 generations on11descendants
  • K182809CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2018 · 4 generations on10descendants
  • K200774CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2020 · 5 generations on5descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K901974Selector Ultrasonic Surgical AspiratorSpembly Medical, Ltd.1990—
+1K042277Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd.2004—
+2K081459Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc.20084
+3K161882CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation20162
+4K182809CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation201842
+5K200774CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200810
200910
201120
201210
201610
201810
201910
202010
202230
202320
202410
202510
202610
FIG. 1 — Lineage of K901974, 1990–2026Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LFL? 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 LFL device

  1. #1 K261448 neXus Ultrasonic Surgical Aspirator Systemscore 14.5 · 10 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (18)

See all 18

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

NumberDeviceApplicantDecidedDescendants
K042277Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd.200417

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?

  • Of its descendants, K042277 (Integra Neurosciences, Ltd., 2004) has gone furthest, with 17 descendants of its own.

How does its category compare?

All LFL devices

LFL Instrument, Ultrasonic Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LFL

3in 2025

2007: 72008: 22009: 12010: 22011: 32012: 32013: 52014: 32015: 42016: 52017: 22018: 32019: 42020: 42021: 62022: 82023: 42024: 32025: 32026 (partial year): 3
2007high 8 (2022) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LFL

176in 2025

2007: 99 days median2011: 241 days median2012: 82 days median2013: 73 days median2014: 136 days median2015: 99 days median2016: 111 days median2018: 66 days median2019: 103 days median2020: 190 days median2021: 83 days median2022: 168 days median2023: 104 days median2024: 158 days median2025: 176 days median2026 (partial year): 99 days median
2007high 241 (2011) · low 66 (2018)2026

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

Recalls per year · LFL

11in 2024

2010: 32011: 22012: 52014: 12015: 12017: 12019: 422021: 12023: 22024: 112026 (partial year): 1
2007high 42 (2019) · low 0 (2007)2026

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

Adverse event reports per year · LFL

3,857in 2025

2007: 2,2362008: 1,6782009: 3,3242010: 1,2392011: 1,0532012: 1,4912013: 2,4302014: 4,2602015: 2,7772016: 2,6912017: 3,2672018: 3,4612019: 3,1532020: 2,9342021: 3,2892022: 3,4222023: 4,2152024: 4,0172025: 3,857
2007high 4,260 (2014) · low 1,053 (2011)2025

MAUDE reports naming product code LFL, 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
200779902,236
20082—01,678
20091—03,324
20102—31,239
2011324121,053
201238251,491
201357302,430
2014313614,260
201549912,777
2016511102,691
20172—13,267
201836603,461
20194103423,153
2020419002,934
202168313,289
2022816803,422
2023410424,215
20243158114,017
2025317603,857
20263991—
Cite this page

510(k) Report. “K901974: Selector Ultrasonic Surgical Aspirator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K901974

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026