CRYPTOCOCCUS NEOFORMANS ANTISERUM, LATEX— 510(k) K792693

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792693 for CRYPTOCOCCUS NEOFORMANS ANTISERUM, LATEX, Substantially Equivalent on 1980-01-21. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code GMD
Advisory panel: Microbiology
Date received: 1979-12-27
Decision date: 1980-01-21
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.