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: LCL FDA unclassified

Radioimmunoassay, Phencyclidine

Unknown

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Radioimmunoassay for phencyclidine (PCP) is a laboratory test method that uses radiolabeled antibodies to detect and measure phencyclidine concentrations in patient specimens, typically for toxicology screening or drug monitoring. This device is currently unclassified by the FDA, with no assigned regulation number or medical specialty, indicating that its classification has not been finalized. The product code is LCL. No special risk flags apply.

510(k) Clearances

11 matches
K Number
Device Name
PSYCHEMEDICS RIA PHENCYCLIDINE ASSAY
AT WORK DRUG TEST, MODEL 9145-25C; MODEL 9177-25C
PCP DIRECT RIA KIT (I-125)
ABUSCREEN FP FOR PHENCYCLIDINE
EMIT HVA PHENCYCLIDINE ASSAY
REVISED LABELING FOR ADX PHENCYCLIDINE
REVISED LABELING FOR SYVA PHENCYCLIDINE ASSAYS
REVISED LABELING FOR TDX PHENCYCLIDINE
ABUSCREEN RADIOIMMUNOASSAY-PHENCYCLIDINE
PHENCYCLIDINE DIRECT BLOOD RIA KIT
ABUSCREEN RIA FOR PHENCYCLIDINE

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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