GEMINI SURGICAL LIGHT— 510(k) K880198

Substantially Equivalent

American Sterilizer Co.

FDA 510(k) clearance K880198 for GEMINI SURGICAL LIGHT, Substantially Equivalent on 1988-02-10. Applicant: American Sterilizer Co..

Clearance details

Applicant: American Sterilizer Co.
Product code: Code FSS
Advisory panel: General, Plastic Surgery
Date received: 1988-01-15
Decision date: 1988-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

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