ANGIOTENSIN CONVERTING ENZYME ASSAY SYS— 510(k) K791712

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K791712 for ANGIOTENSIN CONVERTING ENZYME ASSAY SYS, Substantially Equivalent on 1979-09-19. Applicant: Ventrex Laboratories, Inc..

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code KQN
Advisory panel: Clinical Chemistry
Date received: 1979-07-31
Decision date: 1979-09-19
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.