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: CFE FDA class 2

Electrophoretic, Lactate Dehydrogenase Isoenzymes

Clinical Chemistry

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The Electrophoretic Lactate Dehydrogenase Isoenzymes Test is a clinical chemistry device that uses electrophoresis to separate the five LDH isoenzyme fractions based on their different electrical charges, enabling identification of the tissue source of elevated LDH activity and improving diagnostic specificity for cardiac, hepatic, and other organ-specific injuries. It is classified as FDA Class 2 (moderate risk), though it is exempt from 510(k) premarket notification. The product code is CFE, regulated under 21 CFR 862.1445, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

28 matches
K Number
Device Name
GELSCAN, MODEL 1206
SPIFE LD-12 KIT, MODEL 3338
SPIFE LD VIS ISOENZYME KIT, MODELS 3450, 3451, AND 3452
HYRAGEL ISO-LDH KIT/HYDRAGEL 15 ISO-LDH KIT
CARDIO REP LD
ACA LACTATE DEHYDROGENASE ISOENZYME 1 (LD1) METHOD
ACA(R) LACTIC DEHYDROGENASE ISOENZYME 1 (LD1) METH
ROCHO ISOMUNE - LD
REP(TM) LD-2 STAT KIT, CAT. NO. 3078
TITAN GEL REP LDH-30 HV
TITAN GEL REP LDH-6 HV
TITAN GEL REP LDH-12 HV
TITAN GEL LDH REP SYSTEM
CK/LD BUFFER (CAT. NO. 5808)
ISOENZYME TEST LD-1
TITAN GEL ISO DOT LDH KIT
CORNING LACTATE DEHYDROPHORETIC ASSAY
CARDIZYME PLUS LD #65094/93
TITAN GEL LDH ISO-ENZYME CONTROL
PARAGON ELECTROPHORESIS LACTATE REAG.KIT
TRANSPHOR TM LD LACTATE DEHYDROGENASE
ROCHE IMMUNOCHEMICAL LD ISOENZY REAGENTS
LDH CLINI GEL KIT
ENZYME STABILIZING REAGENT (ESR)
LDH ISOENZYME REAGENT
LDH ISOENZYME REAGENT
LDH ISOENZYME REAGENT
LACTATE DEHYDROGENASE COLORIMETRIC SUB.

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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