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: LCM FDA unclassified

Enzyme Immunoassay, Phencyclidine

Unknown

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Enzyme immunoassay for phencyclidine (PCP) is a laboratory immunoassay test used to detect phencyclidine, a dissociative drug, in patient specimens for clinical toxicology screening or confirmation purposes. This device is currently unclassified by the FDA, with no assigned regulation number or medical specialty designation, meaning its regulatory requirements have not been definitively established. The product code is LCM. No special risk flags apply.

510(k) Clearances

50+ matches
K Number
Device Name
Psychemedics Homogeneous Enzyme Immunoassay (HEIA) for Phencyclidine in Hair
SEFRIA PCP Oral Fluid Enzyme Immunoassay
Immunalysis SEFRIA PCP Oral Fluid Enzyme Immunoassay
Atellica CH Phencyclidine (Pcp)
Immunalysis PCP Urine Enzyme Immunoassay, Immunalysis Multi-Drug Calibrators
CR3 KEYLESS SPLIT SAMPLE CUP PHENCYCLIDIEN - METHYLENEDIOXYMETHAMPHETAMINE
OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY PHENCYCLIDINE
RAPIDFRET ORAL FLUID ASSAY FOR PCP, PCP CALIBRATOR SET, PCP CONTROL SET AND RAPIDEASE ORAL FLUID COLLECTOR
PSYCHEMEDICS PHENCYCLIDINE EIA
THERMO SCIENTIFIC CEDIA PHENCYCLIDINE (PCP) OFT ASSAY
ORAL FLUID PHENCYCLIDINE
OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY FOR PHENCYCLIDINE
RAPIDSENSE DRUGS OF ABUSE PHENCYCLIDINE (PCP) 25 DEVICE WITH MODELS 900-0054
VITROS CHEMISTRY PRODUCTS PCP REAGENT, CALIBRATOR KIT 26, FS CALIBRATOR 1, DAT PERFORMANCE VERIFIERS I, II, III, IV, & V
ACRO RAPID PHENCYCLIDINE URINE TEST, CATALOG PCP001000
QUEST DIAGNOSTICS HAIRCHECK-DT (PCP
RANDOX PHENCYCLIDINE ASSAY
ONLINE DAT PHENCYCLIDINE PLUS
QUICKSCREEN, MODELS 9177X AND 9178X
AMEDICA DRUG SCREEN PHENCYCLIDINE TEST
PHENCYCLIDINE ENZYME IMMUNOASSAY, CATALOG NUMBERS 0010 & 0011
PHENCYCLIDINE
AMEDITECH IMMUTEST DRUG SCREEN PCP
ACON PCP ONE-STEP PHENCYCLIDINE TEST STRIP, ACON PCP ONE-STEP PHENCYCLIDINE TEST DEVICE
LIVESURE PHENECYCLINE (PCP) SCREEN TESTS
INSTANT-VIEW PHENCYCLIDINE (PCP) URINE DIP STRIP TEST
INSTANT-VIEW PHENCYCLIDINE (PCP) URINE CASSETTE TEST
MODIFICATION TO THE EMIT II PLUS PHENCYCLIDINE ASSAY, MODEL OSR9J229
AT HOME DRUG TEST, MODEL 9133 T
BRANAN MEDICAL CORPORATION MONITECT PCP DRUG SCREEN TEST, MODEL 160C AND 160D
MODIFICATION TO PROFILE -II
STC PCP INTERCEPT MICRO-PLATE EIA, MODEL 11541
SCREENERS PHENCYCLIDINE (PCP) TEST, DRUGSCREEN DIP PHENCYCLIDINE (PCP) TEST
URINE PHENCYCLIDINE (PCP) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 94A
ONTRAK TESTSTIK FOR PCP, CAT. 07 6654 2
ONTRAK TESTCUP 5, CAT. 07 6481 7
SYVA EMIT II PLUS PHENCYCLIDINE ASSAY, MODEL 9J029UL
ONTRAK TESTCUP 5 M2K, CAT. 11 1850 1
AT HOME DRUG TEST, MODEL 9133
BIONIKE AQ PHENCYCLIDINE (PCP) TEST
REDI-TEST PCP
MICRO-STRIP FOR PHENCYCLIDINE METABOLITES
VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE
ONE STEP URINE DRUG OF ABUSE: PHENCYCLIDINE (PCP) TEST
AUTO-LYTE PCP EIA, MODEL #1254U
QUIKPAC II ONE STEP PHENCYCLIDINE (PCP) TEST
QUIKSTRIP ONE STEP PHENCYCLIDINE (PCP) TEST
QUICKSCREEN ONE STEP PCP SCREENING TEST
MODIFIED CEDIA DAU PCP ASSAY
ONTRAK TESTCUP 5 (MODIFICATION)

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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