Eskachem, Ck-Mb Reagent

FDA 510(k) K792023 · Smithkline Diagnostics, Inc.

Substantially Equivalent

510(k) numberK792023

Submission

Device name
Eskachem, Ck-Mb Reagent
Applicant
Smithkline Diagnostics, Inc.
Mchenry, IL, US
Received
October 9, 1979
Decision date
October 30, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JHS – Differential Rate Kinetic 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 Eskachem, Ck-Mb Reagent cleared by the FDA?

Eskachem, Ck-Mb Reagent (K792023) received a 510(k) decision of Substantially Equivalent on October 30, 1979, 21 days after the submission was received.

What is the product code of K792023?

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