HEMAGEN CARDIOLIPIN ANTIBODY KIT (EIA METHOD0— 510(k) K932373

Substantially Equivalent

Hemagen Diagnostics, Inc.

FDA 510(k) clearance K932373 for HEMAGEN CARDIOLIPIN ANTIBODY KIT (EIA METHOD0, Substantially Equivalent on 1993-07-16. Applicant: Hemagen Diagnostics, Inc..

Clearance details

Applicant: Hemagen Diagnostics, Inc.
Product code: Code MID
Advisory panel: Immunology
Date received: 1993-05-17
Decision date: 1993-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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