Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: JHW FDA class 2

U.V. Method, Cpk Isoenzymes

Clinical Chemistry

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UV Method for CPK Isoenzymes is a clinical chemistry test system employing ultraviolet spectrophotometric detection to measure creatine kinase isoenzyme activities in serum, used in cardiac and muscular disease diagnosis. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification and compliance with general and special controls. The product code is JHW, regulated under 21 CFR 862.1215, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

27 matches
K Number
Device Name
Creatine Kinase-MB
ELITECH CLINICAL SYSTEMS ENVOY 500 CK REAGENT KIT
ELITECH CLINICAL SYSTEMS CK NAC SL
WIENER LAB. CK-MB DS UV UNITEST, MODEL 28 X 2.5 ML CAT. NR. 1271354
ROCHE DIAGNOSTICS CK-MB
ELECSYS CK-MB
CK-MB METHOD FOR THE TECHNICON IMMUNO 1(R) SYSTEM IN-VITRO DIAGNOSTIC SYSTEM
LIFESIGN, CARE POINT, VITALSIGN, ACCUSIGN
CREATINE KINASE MB DETERMINATION (UV)
AXSYM CK-MB
CARDIO REP CK ISOENZYME KIT - 3310
STAMBI-CK
PROPOSED NEW USE OF INSTRUMENT SYSTEM AND TEST KIT
CREATINE KINASE UV REAGENT SET
LABELLING CHANGES TO IMPRES-MB-X
ISOFOR-MM (TM)
IMPRES-MB
DSL 1700
CARDIOZYME PLUS CK-MB ITEM #65045 (G)
CARDIOZYME PLUS CK-MB ITEM #65045
CREATINE KINASE MB ISOENZYME IMMUNO UV
ISOMUNE-CK
CARDIO ZYME PLUS CK-MB #65045
CREATINE PHOSPHOKINASE (CPK) REAGENT SET
A-GENT CK-MB
CPK ISOENZYME REAGENT
DYNAZYME TM II CARDIAK-MB

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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