510(k) Report

510(k) · Cleared

Cleared

Trypsin 1%

K771955510(k) TraditionalCleared Nov 22, 197736-day reviewClass I21 CFR 864.4400

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

Flow Laboratories, Inc. · IBG Trypsin

Cleared on Nov 22, 1977 after a 36-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
Nov 22, 1977
Review
36 days
Class
Class I
Product code
IBG
Recalls
None
Predicates
0

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

Descendants, by year cleared 2007: 1 descendant cleared19801990200020102020
  1. This deviceK771955 Trypsin 1%Flow Laboratories, Inc. · 1977
  2. Descendant · cites it directly · 0 of its ownK063235 Cytori Lipoplasty System with Celase ReagentCytori Therapeutics, Inc. · 2007

Most influential descendants

Showing 1 of 1 · See all
  • K063235Cytori Lipoplasty System with Celase ReagentCytori Therapeutics, Inc. · 2007 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K771955Trypsin 1%Flow Laboratories, Inc.1977—
+1K063235Cytori Lipoplasty System with Celase ReagentCytori Therapeutics, Inc.2007—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K771955, 1977–2007Source: 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.

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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? (1)

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

NumberDeviceApplicantDecidedDescendants
K063235Cytori Lipoplasty System with Celase ReagentCytori Therapeutics, Inc.20070

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, K063235 (Cytori Therapeutics, Inc., 2007) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IBG devices

IBG Trypsin: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IBG

FDA has decided no IBG device since 2007.

Median 510(k) review, days · IBG

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

Recalls per year · IBG

No recall names IBG since 2007.

Adverse event reports per year · IBG

No MAUDE report names IBG since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K771955: Trypsin 1%.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K771955

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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