ANTI-ENDOMYSIAL ANTIBODY TEST— 510(k) K912551

Substantially Equivalent

Immco Diagnostics, Inc.

FDA 510(k) clearance K912551 for ANTI-ENDOMYSIAL ANTIBODY TEST, Substantially Equivalent on 1993-06-09. Applicant: Immco Diagnostics, Inc..

Clearance details

Applicant: Immco Diagnostics, Inc.
Product code: Code DBL
Advisory panel: Immunology
Date received: 1991-06-11
Decision date: 1993-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo, NY, US

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