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: GNC FDA class 2

Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp.

Microbiology

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The Febrile Antigens for Salmonella Species (All Groups, Slide and Tube Tests) are agglutination reagents used in the serological diagnosis and typing of Salmonella infections, supporting the investigation of typhoid fever and non-typhoidal salmonellosis. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket clearance. The product code is GNC, regulated under 21 CFR 866.3550 in the Microbiology specialty.

510(k) Clearances

50+ matches
K Number
Device Name
VISTA ANTIGEN SALMONELLA H A
VISTA ANTIGEN SALMONELLA O GROUP A
VISTA ANTIGEN SALMONELLA O GROUP D
VISTA ANTIGEN SALMONELLA O GROUP B
VISTA ANTIGEN SALMONELLA H D
VISTA ANTIGEN SALMONELLA H C
VISTA ANTIGEN SALMONELLA H B
VISTA ANTIGEN SALMONELLA O GROUP C
SAS SPICER-EDWARDS 2 ANTISERUM
SAS SPICER-EDWARDS 3 ANTISERUM
SAS SPICER-EDWARDS 4 ANTISERUM
SAS SPICER-EDWARDS EN COMPLEX ANTISERUM
SAS SPICER-EDWARDS 1 ANTISERUM
SAS SPICER-EDWARDS L COMPLEX
SAS SALMONELLA H E COMPLEX ANTISERUM
SAS SALMONELLA H Z38 ANTISERUM
SAS SALMONELLA H FACTOR 5 ANTISERUM
SAS SALMONELLA H 1,7 ANTISERUM
SAS SALMONELLA H E,N,Z15 ANTISERUM
SAS SALMONELLA H POLY D ANTISERUM
SAS SALMONELLA H FACTOR 6 ANTISERUM
SAS SALMONELLA H POLY E ANTISERUM
SAS SALMONELLA H Z36 ANTISERUM
SAS SALMONELLA H FACTOR 7 ANTISERUM
SAS SALMONELLA H 1,2 ANTISERUM
SAS SALMONELLA E,N,X ANTISERUM
SAS SALMONELLA H A ANTISERUM
SAL SALMONELLA H Q ANTISERUM
SAS SALMONELLA H K ANTISERUM
SAS SALMONELLA H Z ANTISERUM
SAS SALMONELLA H H ANTISERUM
SAS SALMONELLA H POLY C ANTISERUM
SAS SALMONELLA H POLY B ANTISERUM
SAS SALMONELLA H T ANTISERUM
SAS SALMONELLA H Z4, Z23 ANTISERUM
SAS SALMONELLA H L,Z40 ANTISERUM
SAS SALMONELLA H L,V ANTISERUM
SAS SALMONELLA H,M,T, ANTISERUM
SAS SALMONELLA H POLY A ANTISERUM
SAS SALMONELLA H I ANTISERUM
SAS SALMONELLA H F,G, ANTISERUM
SAS SALMONELLA H S ANTISERUM
SAS SALMONELLA H Y ANTISERUM
SAS SALMONELLA H L,Z13 ANTISERUM
SAS SALMONELLA H Z29 ANTISERUM
SAS SALMONELLA H R ANTISERUM
SAS SALMONELLA H G,M ANTISERUM
SAS SALMONELLA H X ANTISERUM
SAS SALMONELLA H L,W ANTISERUM
SAS SALMONELLA H Z6 ANTISERUM

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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