IN VITRO DIGOXIN RIA TEST— 510(k) K772110

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K772110 for IN VITRO DIGOXIN RIA TEST, Substantially Equivalent on 1977-11-22. Applicant: Clinical Assays, Inc..

Clearance details

Applicant: Clinical Assays, Inc.
Product code: Code DNL
Advisory panel: Clinical Toxicology
Date received: 1977-11-07
Decision date: 1977-11-22
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.