Creatine Kinase-Mb Kit

FDA 510(k) K820812 · Calbiochem-Behring Corp.

Substantially Equivalent

510(k) numberK820812

Submission

Device name
Creatine Kinase-Mb Kit
Applicant
Calbiochem-Behring Corp.
Walker, MI, US
Received
March 23, 1982
Decision date
April 12, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHY – Colorimetric Method, Cpk Or Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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Questions and answers

When was Creatine Kinase-Mb Kit cleared by the FDA?

Creatine Kinase-Mb Kit (K820812) received a 510(k) decision of Substantially Equivalent on April 12, 1982, 20 days after the submission was received.

What is the product code of K820812?

The FDA product code is JHY – Colorimetric Method, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.