IN-VITRO TEST FOR THE DETERMINATION OF CREATININE— 510(k) K854178

Substantially Equivalent

Clinical Data, Inc.

FDA 510(k) clearance K854178 for IN-VITRO TEST FOR THE DETERMINATION OF CREATININE, Substantially Equivalent on 1985-11-25. Applicant: Clinical Data, Inc..

Clearance details

Applicant: Clinical Data, Inc.
Product code: Code CGX
Advisory panel: Clinical Chemistry
Date received: 1985-10-15
Decision date: 1985-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

Download summary PDF View on FDA.gov ↗

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