RADIAL IMMUNO-TEST FOR HUMAN C-REACTI— 510(k) K831958

Substantially Equivalent

Kent Laboratories, Inc.

FDA 510(k) clearance K831958 for RADIAL IMMUNO-TEST FOR HUMAN C-REACTI, Substantially Equivalent on 1983-07-19. Applicant: Kent Laboratories, Inc..

Clearance details

Applicant: Kent Laboratories, Inc.
Product code: Code DCK
Advisory panel: Immunology
Date received: 1983-06-17
Decision date: 1983-07-19
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.