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Karl Storz Semi-Rigid Micro-Endoscopes & Accessories for Endosccopic Gynecological Surgical Procedures

by Karl Storz Endoscopy-America, Inc.

510(k) K951343

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK951343 Date11 Apr 1996ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-1473-2024 FDA Class II initiated 27 Feb 2024

    Inadequate reprocessing validation evidence

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
HET
Device Class
Class II
Regulation
21 CFR Part 884.1720
Advisory Committee
Obstetrics/Gynecology
FDA Decision
SESE Substantially Equivalent

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