TIA CRP TEST KIT— 510(k) K914155

Substantially Equivalent

Crestat Diagnostics, Inc.

FDA 510(k) clearance K914155 for TIA CRP TEST KIT, Substantially Equivalent on 1992-01-15. Applicant: Crestat Diagnostics, Inc..

Clearance details

Applicant: Crestat Diagnostics, Inc.
Product code: Code DCK
Advisory panel: Immunology
Date received: 1991-09-16
Decision date: 1992-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

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