510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K936231Substantially Equivalent

The Karl Storz Hamou Endomat

Karl Storz Endoscopy-America, Inc., Culver City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K936231 is the FDA 510(k) clearance record for THE KARL STORZ HAMOU ENDOMAT, a class II device, cleared for Karl Storz Endoscopy on under FDA product code HIG (Insufflator, Hysteroscopic). FDA records list 402 510(k) clearances for KARL STORZ ENDOSCOPY-AMERICA, INC., from to . As of , FDA records show no recalls naming K936231.

Clearance record

Decision date
Received
(391 days to decision)
Product code
HIG Insufflator, Hysteroscopic
Regulation
21 CFR 884.1700
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Karl Storz Endoscopy 600 Corporate Pt.e, Culver City CA
510(k) summary
Summary
Third party review
No

Clearances, product code HIG

Trailing 12 months
2 clearances under product code HIG in the twelve months to November 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HIG, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260