HISTOPLASMA CAPSULATUM, ANTIGEN— 510(k) K792701

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792701 for HISTOPLASMA CAPSULATUM, ANTIGEN, Substantially Equivalent on 1980-01-23. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code GMJ
Advisory panel: Microbiology
Date received: 1979-12-27
Decision date: 1980-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.