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: GNB FDA class 2

Antisera, All Types, Shigella Spp.

Microbiology

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The Antisera for All Types of Shigella Species are serotyping reagents used in microbiology laboratories to identify and classify Shigella isolates responsible for bacterial dysentery (shigellosis), a significant cause of diarrheal disease worldwide. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket clearance. The product code is GNB, regulated under 21 CFR 866.3660 in the Microbiology specialty.

510(k) Clearances

41 matches
K Number
Device Name
SAS SHIGELLA SONNEI FORM II ANTISERUM
SAS SHIGELLA BOYDII TYPE 9 ANTISERUM
SAS SHIGELLA BOYDII TYPE 12 ANTISERUM
SAS SHIGELLA SONNEI FORM I ANTISERUM (3/100/1000ML)
SAS SHIGELLA FLEXNERI TYPE 1 ANTISERUM
SAS SHIGELLA SONNEI GROUP D ANTISERUM
SAS SHIGELLA DYSENTERIAE GROUP A1 (8-10) ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 8 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 10 ANTISERUM
SAS SHIGELLA FLEXNERI TYPE 4 ANTISERUM
SAS SHIGELLA BOYDII TYPE 8 ANTISERUM
SAS SHIGELLA BOYDII TYPE 13 ANTISERUM
SAS SHIGELLA BOYDII GROUP C1/C1 (8-10) ANTISERUM
SAS SHIGELLA BOYDII TYPE 14 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 1 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 9 ANTISERUM
SAS SHIGELLA FLEXNERI TYPE 2 ANTISERUM
SAS SHIGELLA BOYDII TYPE 15 ANTISERUM
SAS SHIGELLA FLEXNERI TYPE 6 ANTISERUM
SAS SHIGELLA FLEXNERI TYPE 3 ANTISERUM
SAS SHIGELLA BOYDII TYPE 10 ANTISERUM
SAS SHIGELLA FLEXNERI TYPE 5 ANTISERUM
SAS SHIGELLA BOYDII TYPE 11 ANTISERUM (3/100/1000ML)
SAS SHIGELLA DYSENTERIAE TYPE 2 ANTISERUM
SAS SHIGELLA DYSENTERIAE GROUP A (1-7) ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 7 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 5 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 6 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 4 ANTISERUM
SAS SHIGELLA DYSENTERIAE TYPE 3 ANTISERUM
SAS SHIGELLA BOYDII TYPE 7 ANTISERUM
SAS SHIGELLA BOYDII TYPE 6 ANTISERUM
SAS SHIGELLA BOYDII TYPE 2 ANTISERUM
SAS SHIGELLA BOYDII TYPE 1 ANTISERUM
SAS SHIGELLA BOYDII TYPE 5 ANTISERUM
SAS SHIGELLA BOYDII TYPE 4 ANTISERUM
SAS SHIGELLA BOYDII TYPE 3 ANTISERUN
SAS SHIGELLA BOYDII GROUP C2 ANTISERUM
WELLCOLEX COLOUR SHIGELLA TEST ZC51
PHADEBACT SHIGELLA TEST
SHIGELLA I.D.

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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