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: GQG FDA class 1

Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

Microbiology

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The Antigen, CF (Including CF Controls), Respiratory Syncytial Virus is a complement fixation (CF) antigen and associated control reagent used in laboratory testing to detect antibodies against RSV in patient serum. It is an FDA Class 1 device subject only to general controls, representing the lowest regulatory risk tier and requiring no premarket approval or 510(k). Regulated under 21 CFR 866.3480, it carries product code GQG and belongs to the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

31 matches
K Number
Device Name
Nano-Check™ RSV Test
Sofia RSV FIA on Sofia 2 analyzer
BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV
BD VERITOR (TM) SYSTEM FOR RAPID DETECTION OF RSV
SOFIA(R) RSV FIA
BD VERITOR(TM) SYSTEM FOR THE RAPID DETECTION OF RSV
QUICKVUE RSV 10
BD DIRECTIGEN EZ RSV
RAMP RSV ASSAY
QUICK VUE RSV TEST, MODELS 20193, 20199
IMMUNOCARD STAT! RSV MODEL #750630
BINAX NOW RSV TEST, MODEL 430-000 AND BINAX NOW NASOPHARYNGEAL SWAB ACCESSORY PACK, MODEL 400-065
SAS RSV TEST
RSV OIA
BD DIRECTIGEN EZ RSV KIT
QUICKLAB RSV
BINAX NOW RSV TEST (27 TEST), BINAX NOW NASOPHARYNGEAL SWAB SPECIMEN ACCESSORY PACK
RSV ANTIGEN CONTROL SLIDES
VIDAS RESPIRATORY SYNCYTIAL VIRUS (RSV) ASSAY
FITC MURINE MONOCLONAL ANTI-RSV IGG
DIRECTIGEN RESPIRATORY SYNCYTIAL VIRUS TEST KIT
ABBOTT TESTPACK(TM) RSV POSITIVE CONTROL
ABBOTT TESTPACK RSV
PATHFINDER(TM) RESPIRATORY SYNCYTIAL VIRUS
ABBOTT RSV EIA
IMAGEN RESPIRATORY SYNCYTIAL VIRUS TEST
RESPIRATORY SYNCYTIAL VIRUS ID REAGENT
RESPIRATORY SYNCYTIAL VIRUS
RESPIRATORY SYNCYTIAL VIRUS ANTIGEN &
RESP. SYNCYTIAL-FA LABELLHD (8-301-RF)
RESP. SYNCYTIAL-FA LABELLED PRESERUM

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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