HISTOPLASMA CAPSULATUM, ANTISERUM— 510(k) K792679

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792679 for HISTOPLASMA CAPSULATUM, ANTISERUM, Substantially Equivalent on 1980-01-17. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code GMK
Advisory panel: Microbiology
Date received: 1979-12-27
Decision date: 1980-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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