ANTI-CARDIOLIPIN ANTIBODY (IGM-ACA) TEST— 510(k) K933788

Substantially Equivalent

Immco Diagnostics, Inc.

FDA 510(k) clearance K933788 for ANTI-CARDIOLIPIN ANTIBODY (IGM-ACA) TEST, Substantially Equivalent on 1995-03-07. Applicant: Immco Diagnostics, Inc..

Clearance details

Applicant: Immco Diagnostics, Inc.
Product code: Code MID
Advisory panel: Immunology
Date received: 1993-08-04
Decision date: 1995-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo, NY, US

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