HEMOLAB PROTEIN C CHROMOGENIC ASSAY— 510(k) K934210

Substantially Equivalent

Biomerieux Vitek, Inc.

FDA 510(k) clearance K934210 for HEMOLAB PROTEIN C CHROMOGENIC ASSAY, Substantially Equivalent on 1994-12-22. Applicant: Biomerieux Vitek, Inc..

Clearance details

Applicant: Biomerieux Vitek, Inc.
Product code: Code GGP
Advisory panel: Hematology
Date received: 1993-08-30
Decision date: 1994-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hazelwood, MO, US

Download summary PDF View on FDA.gov ↗

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