IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN— 510(k) K831961

Substantially Equivalent

Kent Laboratories, Inc.

FDA 510(k) clearance K831961 for IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN, Substantially Equivalent on 1983-08-11. Applicant: Kent Laboratories, Inc..

Clearance details

Applicant: Kent Laboratories, Inc.
Product code: Code JBQ
Advisory panel: Hematology
Date received: 1983-06-17
Decision date: 1983-08-11
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.