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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: MVO FDA unclassified

Kit, Test, Multiple, Drugs Of Abuse, Over The Counter

Unknown

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A Multiple Drugs of Abuse Over-the-Counter Test Kit is an in vitro diagnostic device intended for consumer (non-prescription) use to screen for the presence of multiple illicit or controlled substances in urine samples. This device has an unclassified status (class "U") in the FDA database. The product code is MVO with no regulation number assigned, and the device is not an implant and is not life-sustaining.

510(k) Clearances

18 matches
K Number
Device Name
ACCU-STAT HOME DRUG TESTS FOR MARIJUANA (THC) AND FOR MARIJUANA & COCAINE (THC, COC)
AT HOME DRUG CUP, MODEL 9150X
LIFESIGN MET, STATUS STIK MET, ACCUSIGN STIK MET, ACCUSTIK MET, ACCUSIGN MET, STATUS DS MET
PEACE OF MIND HOME DRUG TEST
AT HOME DRUG TEST, MODEL 9069
AT HOME DRUG TEST, MODEL 9064
AT HOME DRUG TEST, MODEL 9074
AT HOME DRUG TEST, MODEL 9078 T
AT HOME DRUG TEST, MODEL 9068 T
AT HOME DRUG TESTT, MODEL 9150 T
AT HOME DRUG TEST, MODEL 9083 T
MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175
DRUG STOP
QUICKSCREEN WORKPLACE DRUG SCREENING TEST, MODEL 9147 25C
AT HOME DRUG TEST, MODEL 9175
AT HOME DRUG TEST, MODEL 9171
AT HOME COCAINE & THC SCREENING TEST, MODEL 9170
QUICKSCREEN AT HOME DRUG TEST, MODEL 9149/9150

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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