IN VITRO T-3 UPTAKE TEST— 510(k) K770480

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K770480 for IN VITRO T-3 UPTAKE TEST, Substantially Equivalent on 1977-04-06. Applicant: Clinical Assays, Inc..

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code KHQ
Advisory panel: Clinical Chemistry
Date received: 1977-03-11
Decision date: 1977-04-06
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.