HEMAGEN RHEUMATOID FACTOR KIT (EIA METHOD)— 510(k) K962836

Substantially Equivalent

Hemagen Diagnostics, Inc.

FDA 510(k) clearance K962836 for HEMAGEN RHEUMATOID FACTOR KIT (EIA METHOD), Substantially Equivalent on 1996-09-12. Applicant: Hemagen Diagnostics, Inc..

Clearance details

Applicant: Hemagen Diagnostics, Inc.
Product code: Code DHR
Advisory panel: Immunology
Date received: 1996-07-22
Decision date: 1996-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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