Titan Gel CPK Isoenzyme System

FDA 510(k) K822124 · Helena Laboratories

Substantially Equivalent

510(k) numberK822124

Submission

Device name
Titan Gel CPK Isoenzyme System
Applicant
Helena Laboratories
Walker, MI, US
Received
July 19, 1982
Decision date
November 1, 1982
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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K904866Coulter Ck-Mb Isoenzyme ReagentJHT · Traditional Coulter Electronics, Inc.12/13/1990SE
K904721DSL Ck-Mb (DSL #3200)JHT · Traditional Diagnostic Systems Laboratories, Inc.12/13/1990SE
K901450Modified Label for Embria-Ck, Quick-Mb/Micromi-MbJHT · Traditional Intl. Immunoassay Laboratories, Inc.05/15/1990SE
K896170Rep CK Isoforms Kit Cat. No. 3081, 3082, 3083JHT · Traditional Helena Laboratories02/16/1990SE
K881168Creatine Kinase (CK) Isoenzyme MBJHT · Traditional Data Medical Associates, Inc.11/10/1988SE
K874284Shot-Gun Isolat Proced/Measurement Ck-Mb in SerumJHT · Traditional Diagnostic Chemicals, Ltd. (Usa)01/21/1988SE
K872041Coulter Dart Ck-Mb Isoenzyme Reagent SystemJHT · Traditional Coulter Electronics, Inc.09/16/1987SE

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Questions and answers

When was Titan Gel CPK Isoenzyme System cleared by the FDA?

Titan Gel CPK Isoenzyme System (K822124) received a 510(k) decision of Substantially Equivalent on November 1, 1982, 105 days after the submission was received.

What is the product code of K822124?

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