KARL STORZ ENDOSCOPY-AMERICA, INC.— 510(k) K933216

Name: FDA 510(k) clearance K933216
Creator: U.S. Food and Drug Administration
Published: 1993-09-09

Substantially Equivalent

KARL STORZ Endoscopy-America, Inc.

FDA 510(k) clearance K933216 for KARL STORZ ENDOSCOPY-AMERICA, INC., Substantially Equivalent on 1993-09-09. Applicant: KARL STORZ Endoscopy-America, Inc.. Device class: 2.

Clearance details

Applicant: KARL STORZ Endoscopy-America, Inc.
Product code: Code FFS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-04-27
Decision date: 1993-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

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