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: GQN FDA class 2

Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2

Microbiology

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The Antigen, CF (Including CF Control), Herpesvirus Hominis 1,2 is a complement fixation antigen with controls used in serological testing to detect antibodies to herpes simplex virus types 1 and 2. As an FDA Class 2 device, it carries moderate risk and requires 510(k) premarket clearance to establish substantial equivalence before it may be marketed. Regulated under 21 CFR 866.3305 with product code GQN, it is reviewed within the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

34 matches
K Number
Device Name
DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION AND TYPING KIT, MODEL 01-090000
DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION KIT, MODEL 01-080000
LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAY
ELVIS HSV ID/TYPING TEST SYSTEM
HSV-1 ANTIGEN CONTROL SLIDES
HSV-2 ANTIGEN CONTROL SLIDES
ELVIS HSV GOLD
ELVIS HSV
HSV IN SITU DNA PROBE HYBRIDIZATION TEST KIT
MODIFIED CELL-MATICS HERPES SIMPLEX VIRUS DETECT.
HERPES VIRUS CONTROL SLIDES
HYBRIWICK SYSTEM: HERPES DNA PROBE TEST KIT
WELLCOZYME HSV WZO2
COLORGENE HSV DNA HYBRIDIZATION TEST
FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG
FITC MURINE MONOCLONAL ANTI-HSV BIVALENT IGG
MICROTRAK HSV CULTURE IDENTIFICATION TEST
DU PONT HERPCHEK HSV ANTIGEN ELISA TEST KIT
RAMP HERPES SIMPLEX VIRUS (HSV) (CCT)
COLORGENE DNA HYBRIDIZATION TEST FOR HSV CONFIRMA.
IMAGEN HERPES SIMPLEX VIRUS (HSV) TYPING TEST
HSV IDR
ORTHO HSV ANTIGEN ELISA TEST
DIRECT ELISA FOR HERPES SIMPLEX VIRUS
IMMUNOPER-OXIDASE TEST KIT FOR DETECT OF
H. SIMPLEX VIRUS
HERPES SIMPLEX GROUP CF ANTIGEN
CORDIA HS ANTIBODY TYPING REAGENTS
MICROTRAKSPECIMAN ID TYPING TEST CONTR
SIMPLEX-2
CORDIA HS
HERPES
HSV BIO-BEAD TITRATION KIT
HSV BIO-BEAD SCREEN KIT

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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