ANGIOTENSIN CONVERTING ENZYME ASSAY SYS— 510(k) K791712

Name: FDA 510(k) clearance K791712
Creator: U.S. Food and Drug Administration
Published: 1979-09-19

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.. Device class: 2.

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code KQN
Device class: Class 2
Regulation: 21 CFR 862.1090
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 ↗

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