510(k) Report

510(k) · Cleared

Cleared

Nezhat-Dorsey Hydro-Dissection Universal Bag Squeezer

K953574510(k) TraditionalCleared Sep 29, 199560-day reviewClass II21 CFR 884.1720

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

American Hydro-Surgical Instruments, Inc. · HET Laparoscope, Gynecologic (And Accessories)

Cleared on Sep 29, 1995 after a 60-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 later devices descend from it.

Decided
Sep 29, 1995
Review
60 days
Class
Class II
Product code
HET
Recalls
None
Predicates
0

6 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 1997: 1 descendant cleared1998: 2 descendants cleared1999: 1 descendant cleared2016: 1 descendant cleared2023: 1 descendant cleared1995200020052010201520202025
  1. This deviceK953574 Nezhat-Dorsey Hydro-Dissection Universal Bag SqueezerAmerican Hydro-Surgical Instruments, Inc. · 1995
  2. Descendant · cites it directly · 5 of its ownK973133 Big Bag 3000 Pressure InfusorByron Medical · 1997
  3. Descendant · cites it directly · 2 of its ownK980738 Psi-Tec Syringe Infusion Pump and Accessories for General Fluid…Byron Medical · 1998
  4. Descendant · 2 generations on · 1 of its ownK153599 Concert Medical Hands-Free Syringe (HFS)Concert Medical, LLC · 2016
  5. Descendant · cites it directly · 1 of its ownK980089 3600 Presure Infusor, Sigmacon 3600, Lapro Flow 3000Valley West, Inc. · 1998
  6. Descendant · 3 generations on · 0 of its ownK230083 SafiraMedovate Limited · 2023

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

1997: 11998: 21999: 12016: 12023: 1
1997high 2 (1998) · low 0 (2000)2026

Most influential descendants

Showing 5 of 6 · See all
  • K973133Big Bag 3000 Pressure InfusorByron Medical · 1997 · cites it directly5descendants
  • K980738Psi-Tec Syringe Infusion Pump and Accessories for General Fluid Irrigaion/InfiltrationByron Medical · 1998 · cites it directly2descendants
  • K153599Concert Medical Hands-Free Syringe (HFS)Concert Medical, LLC · 2016 · 2 generations on1descendant
  • K9800893600 Presure Infusor, Sigmacon 3600, Lapro Flow 3000Valley West, Inc. · 1998 · cites it directly1descendant
  • K230083SafiraMedovate Limited · 2023 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K953574Nezhat-Dorsey Hydro-Dissection Universal Bag SqueezerAmerican Hydro-Surgical Instruments, Inc.1995—
+1K973133Big Bag 3000 Pressure InfusorByron Medical1997—
+1K980738Psi-Tec Syringe Infusion Pump and Accessories for General Fluid…Byron Medical1998—
+2K153599Concert Medical Hands-Free Syringe (HFS)Concert Medical, LLC2016—
+1K9800893600 Presure Infusor, Sigmacon 3600, Lapro Flow 3000Valley West, Inc.1998—
+3K230083SafiraMedovate Limited2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
199820
199910
201610
202310
FIG. 1 — Lineage of K953574, 1995–2023Source: 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 HET? 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 HET device

  1. #1 K250939 SIRIUS Endoscope System (PR-SI-1230)score 12.9 · 11 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? (6)

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

NumberDeviceApplicantDecidedDescendants
K973133Big Bag 3000 Pressure InfusorByron Medical19975
K980738Psi-Tec Syringe Infusion Pump and Accessories for General Fluid Irrigaion/InfiltrationByron Medical19982
K9800893600 Presure Infusor, Sigmacon 3600, Lapro Flow 3000Valley West, Inc.19981
K9904471000 Pressure Infusion Sigmacon 1000Valley West, Inc.19990

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, K973133 (Byron Medical, 1997) has gone furthest, with 5 descendants of its own.

How does its category compare?

All HET devices

HET Laparoscope, Gynecologic (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HET

2in 2025

2008: 32009: 12010: 12011: 22012: 22013: 22015: 22017: 22018: 12019: 22020: 22021: 42022: 12025: 2
2007high 4 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HET

269in 2021

2008: 176 days median2021: 269 days median
2007high 269 (2021) · low 176 (2008)2026

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

Recalls per year · HET

4in 2023

2008: 42009: 12015: 12022: 12023: 4
2007high 4 (2008) · low 0 (2007)2026

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

Adverse event reports per year · HET

4,513in 2025

2007: 1812008: 3592009: 4032010: 2142011: 4172012: 1,1182013: 1,0352014: 1752015: 1242016: 2052017: 892018: 532019: 442020: 492021: 1322022: 2162023: 8242024: 3,4962025: 4,513
2007high 4,513 (2025) · low 44 (2019)2025

MAUDE reports naming product code HET, 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
20070—0181
200831764359
20091—1403
20101—0214
20112—0417
20122—01,118
20132—01,035
20140—0175
20152—1124
20160—0205
20172—089
20181—053
20192—044
20202—049
202142690132
20221—1216
20230—4824
20240—03,496
20252—04,513
20260—0—
Cite this page

510(k) Report. “K953574: Nezhat-Dorsey Hydro-Dissection Universal Bag Squeezer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K953574

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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