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: GIR FDA class 1

Reagent, Russel Viper Venom

Hematology

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Reagent, Russell Viper Venom (product code GIR) is a hematology reagent derived from Russell's viper venom that activates Factor X directly, used in coagulation tests such as the dilute Russell viper venom time (dRVVT) to detect lupus anticoagulants and investigate coagulation pathway abnormalities. This device is classified as FDA Class 1, the lowest risk category, and requires 510(k) premarket notification. Regulated under 21 CFR 864.8950 in the Hematology specialty (HE), it is eligible for third-party review.

510(k) Clearances

16 matches
K Number
Device Name
REAGENT, RUSSEL VIPER VENOM - LA SCREEN
REAGENT, RUSSEL VIPER VENOM - LA CONFIRM
HEMOSIL DRVVT SCREEN & HEMOSIL DRVVT CONFIRM
LUPOTEK CORRECTIN VL, LUPOTEK DETECTIN VL, PLASMACON LA
STA - STACLOT DRVV SCREEN; STA - STACLOT DRVV CONFIRM
ACCUCLOT DRVVT CONFIRM, CATALOG NO. A62119
ACCUCLOT DRVVT SCREEN, CATALOG NO. A6094
CRYOCHECK LA SURE, MODEL SUR25-10
CRYOCHECK LA CHECK, MODELS CHK25-10 (25 X1.0 ML), CHK80-10 (80 X 1.0 ML)
IL TEST LAC SCREEN (CLAIMS ADDED TO ACL FUTURA), IL TEST LAC CONFIRM (CLAIMS ADDAD TO ACL FUTURA)
DV TEST AND DVV CONFIRM
BIOCLOT LA
LUPO-TEST REGEANT
LUCOR CONFIRMATORY REAGENT
LUPO-TEST REAGENT
DIA REPTIN

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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