RELIEF— 510(k) K812567

Substantially Equivalent

American Pharmaceutical Co., Inc.

FDA 510(k) clearance K812567 for RELIEF, Substantially Equivalent on 1981-11-10. Applicant: American Pharmaceutical Co., Inc..

Clearance details

Applicant: American Pharmaceutical Co., Inc.
Product code: Code LKX
Advisory panel: Unknown
Date received: 1981-09-09
Decision date: 1981-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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