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: CEP FDA class 1

Radioimmunoassay, Luteinizing Hormone

Clinical Chemistry

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The Luteinizing Hormone Radioimmunoassay is a clinical chemistry device that uses radiolabeled antibody techniques to measure luteinizing hormone (LH) levels in serum, used in the assessment of reproductive endocrine function, diagnosis of infertility, and evaluation of pituitary disorders. It is classified as FDA Class 1 (lowest risk), subject only to general controls, and is exempt from premarket notification. The product code is CEP, regulated under 21 CFR 862.1485, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
MAYBE?MOM MINI OVULATION MICROSCOPE
INSTANT-VIEW LH OVULATION PREDICTING TEST
AT HOME OVULATION TEST, MODEL 9032
CLEARPLANE EASY OVULATION TEST
TCI-31 LIFELONG OVULATION TESTER
QUIK-CHECK OVULATION PREDICTOR
SURE CHECK OVULATION PREDICTOR
INVERNESS MEDICAL OVULATION PREDICTOR TEST
EARLY OVULATION PREDICTOR (CASSETTE), ONE STEP OVULATION PREDICTOR (CASSETTE), OVULATION PREDICTOR (CASSETTE)
EARLY OVULATION PREDICTOR (STICK), ONE STEP OVULATION PREDICTOR (STICK), OVULATION PREDICTOR (STICK)
OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031
BESURE PLUS ONE-STEP HOME OVULATION PREDICTOR KIT
CLEARPLAN EASY OVULATION TEST
DBEST ONE-STEP OVULATION TEST
TBD* ONE-STEP OVULATION PREDICTOR TEST
EZ SURE ONE STEP OVULATION PREDICTOR HOME TEST KIT
VITROS IMMUNODIAGNOSTICS PRODUCTS LH REAGENT PACK (GEM.1055) AND LH CALIBRATORS (GEM.CO55)
ELECSYS LH ASSAY
SEALITE SCIENCES, INC. AQUALITE LH
OVUSIGN - ONE-STEP HOME OVULATION PREDICTOR TEST
OPUS HLH
ACS LH2 IMMUNOASSAY
MINICLINIC OVULATION PREDICTOR
ACTIVE LH IRMA
FIRST RESPONSE OVULATION PREDICTOR TEST
CONCEIVE OVULATION PREDICTOR
BESURE ONE-=STEP HOME OVULATION PREDICTOR KIT
COAT-A-COUNT LH IRMA
CHEMILUMINESCENCE LH
PRO-STEP LH OVULATION PREDICTION TEST
SEALITE SCIENCE, INC. AQUALITE(R) LH
DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD
SIMULTRAC LH/FSH RADIOUMMUNOASSAY KIT
ACCESS(R) HUMAN LUTEINZING HORMONE ASSAY
ONE STEP LH TEST
COBAS CORE LH EIA
VISTA(R) HUMAN LUTEINIZING HORMONE(HLH) ASSAY
OVUSIGN LH/CONCEPTION PLUS/OVUDATE LH ONE-STEP
IMMUCHEM LH-MW ELISA
ELISA TUBE LH TEST KIT
VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM
IMMULITE HLH
LH GEN III SELF-TEST/CONCEIVE
MEDIX BIOTECH LH ENZYME IMMUNOASSAY TEST KIT
OPUS(R) LH TEST SYSTEM
LH IRMA IMMUNOMAG
MINICLINIC OVULATION PREDICTION TEST
PANTEX IRMA LH 1251 KIT
CIBA CORNING ACS LH IMMUNOASSAY
BIOCLONES ELEGANCE LH ELISA KIT

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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