ANTI-GLOBULIN CONTROL— 510(k) K792695

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792695 for ANTI-GLOBULIN CONTROL, Substantially Equivalent on 1980-01-24. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code DHR
Advisory panel: Immunology
Date received: 1979-12-27
Decision date: 1980-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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