AUTOANTIBODY TEST SYSTEM (MOUSE KIDNEY/STOMACH)— 510(k) K883915

Substantially Equivalent

Immco Diagnostics, Inc.

FDA 510(k) clearance K883915 for AUTOANTIBODY TEST SYSTEM (MOUSE KIDNEY/STOMACH), Substantially Equivalent on 1988-10-19. Applicant: Immco Diagnostics, Inc..

Clearance details

Applicant: Immco Diagnostics, Inc.
Product code: Code DBL
Advisory panel: Immunology
Date received: 1988-09-16
Decision date: 1988-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo, NY, US

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