510(k) Report

510(k) · Cleared

Cleared

Mullan Ganglion Microcompression Set

K940973510(k) TraditionalCleared Sep 29, 1995575-day reviewClass I21 CFR 882.4535

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

Cook, Inc. · HAO Instrument, Surgical, Non-Powered

Cleared on Sep 29, 1995 after a 575-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Sep 29, 1995
Review
575 days
Class
Class I
Product code
HAO
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2022: 1 descendant cleared1995200020052010201520202025
  1. This deviceK940973 Mullan Ganglion Microcompression SetCook, Inc. · 1995
  2. Descendant · cites it directly · 0 of its ownK220920 Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K940973Mullan Ganglion Microcompression SetCook, Inc.1995—
+1K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co., Ltd.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K940973, 1995–2022Source: 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 HAO? 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 HAO device

  1. #1 K220920 Matreneu Percutaneous Balloon Compression Kitscore 4.0 · 1 generation · no Class I recall
Get a 510(k) Report

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? (1)

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

NumberDeviceApplicantDecidedDescendants
K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co., Ltd.20220

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, K220920 (Shenzhen Shineyard Medical Device Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HAO devices

HAO Instrument, Surgical, Non-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HAO

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HAO

Too few HAO 510(k)s in any year since 2007 to give a median.

Recalls per year · HAO

1in 2011

2010: 12011: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · HAO

8in 2025

2007: 12008: 32009: 152010: 302011: 62012: 152013: 62014: 122015: 672016: 552017: 262018: 102019: 192020: 72021: 102022: 102023: 122024: 62025: 8
2007high 67 (2015) · low 1 (2007)2025

MAUDE reports naming product code HAO, 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—01
20080—03
20090—015
20100—130
20110—16
20120—015
20130—06
20140—012
20150—067
20160—055
20170—026
20180—010
20190—019
20200—07
20210—010
20221—010
20230—012
20240—06
20250—08
20260—0—
Cite this page

510(k) Report. “K940973: Mullan Ganglion Microcompression Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K940973

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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