DeviceClearance

IV VITRO GAMMADAB T4 RIA KIT— 510(k) K781235

Substantially Equivalent

Clinical Assays, Inc.

FDA 510(k) clearance K781235 for IV VITRO GAMMADAB T4 RIA KIT, Substantially Equivalent on 1978-08-14. Applicant: Clinical Assays, Inc..

Clearance details

Applicant
Clinical Assays, Inc.
Product code
Code CDX
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

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