ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY— 510(k) K820616

Substantially Equivalent

E. R. Squibb & Sons, Inc.

FDA 510(k) clearance K820616 for ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY, Substantially Equivalent on 1982-03-26. Applicant: E. R. Squibb & Sons, Inc..

Clearance details

Applicant: E. R. Squibb & Sons, Inc.
Product code: Code CIB
Advisory panel: Clinical Chemistry
Date received: 1982-03-08
Decision date: 1982-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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