RPR TEST FOR SYPHILIS IN SERUM OR PLASMA— 510(k) K880477

Substantially Equivalent

Ampcor, Inc.

FDA 510(k) clearance K880477 for RPR TEST FOR SYPHILIS IN SERUM OR PLASMA, Substantially Equivalent on 1988-03-30. Applicant: Ampcor, Inc..

Clearance details

Applicant: Ampcor, Inc.
Product code: Code GMQ
Advisory panel: Microbiology
Date received: 1988-02-04
Decision date: 1988-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bridgeport, NJ, US

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