STORZ MODEL 62 ENT CAMERA SYSTEM— 510(k) K883760

Name: FDA 510(k) clearance K883760
Creator: U.S. Food and Drug Administration
Published: 1988-09-28

Substantially Equivalent

Storz Instrument Co.

FDA 510(k) clearance K883760 for STORZ MODEL 62 ENT CAMERA SYSTEM, Substantially Equivalent on 1988-09-28. Applicant: Storz Instrument Co.. Device class: 1.

Clearance details

Applicant: Storz Instrument Co.
Product code: Code FWL
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1988-09-06
Decision date: 1988-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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