CPK Clini Gel Kit

FDA 510(k) K791826 · Clinical Sciences, Inc.

Substantially Equivalent

510(k) numberK791826

Submission

Device name
CPK Clini Gel Kit
Applicant
Clinical Sciences, Inc.
Mchenry, IL, US
Received
September 17, 1979
Decision date
October 1, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHT – Chromatographic Separation, Cpk Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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Questions and answers

When was CPK Clini Gel Kit cleared by the FDA?

CPK Clini Gel Kit (K791826) received a 510(k) decision of Substantially Equivalent on October 1, 1979, 14 days after the submission was received.

What is the product code of K791826?

The FDA product code is JHT – Chromatographic Separation, Cpk Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.