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: JTO FDA class 1

Discs, Strips And Reagents, Microorganism Differentiation

Microbiology

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Discs, Strips and Reagents, Microorganism Differentiation are microbiological reagent products used to perform biochemical differentiation tests that distinguish between closely related microbial species or genera based on enzymatic or metabolic reactions. It is classified as FDA Class 1, posing the lowest risk and subject to general controls only. The product code is JTO, regulated under 21 CFR 866.2660, and falls within the Microbiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT
PYR SWAB
GRAM SWAB
INDOLE SWAB
LYFO(TM) DIFFERENTIAL DISK-BACITRACIN
IDS RAPID CB PLUS SYSTEM
COLISCREEN
M. CAT BUTYRATE DISK
GIBSON ID-M. CAT.
DRYSLIDE CARTARRHALIS
LYFO(TM) DIFFERIENTAL DISK-PYR
GIBSON ID A.E. TEST
LYFO(TM) DIFFERENTIAL DISK
B-L RED(TM) DISCS
LYFO(TM) DIFFERENTIAL DISK-BILE ESCULIN
LYFO(TM) DIFFERENTIAL DISK-SPS
LYFO(TM) DIFFERENTIAL DISK-STERILE DISK
LYFO(TM) DIFFERENTIAL DISK-BILE
SWABZYME OXIDASE
GONOCHEK II REAGENT TUBES
GONOCHEK-II, MODIFICATION
B-LACTAMASE REAGENT TUBES
STREP-A-CHEK(TM) REAGENT STRIPS
STREP-A-CHEK
EY-20 REAGENT TUBES
STREP-SURE A/E
DISPENS-O-DISC(TM) NITROCEFIN
BACTICARD STREP
SERIM PYLORITEK REAGENT STRIPS
BACTICARD E. COLI
PYR TEST KIT
VISI-SPOT
BACTICARD STREP
NINHYDRIN REAGENT
CATALASE REAGENT
OXYSTRIP
BACTIDROP(TM) MUCAP
FERRIC CHLORID REAGENT, 10%
INDOLE SPOT & INDOLE KOVACS REAGENT
NITRATE REAGENTS A, B AND C
VOGUES-PROSKAUER REAGENT A & B
BBL NITRATE A, B REAGENT DROPPERS
BBL NINHYDRIN REAGENT DROPPERS
BBL PYR REAGENT DROPPERS
DRYSLIDE(TM) INDOLE
INDOXYL ACETATE DISK
LAP DISK
BACTIDROP INDOLE (ERLICH'S)
DRYSLIDE(TM), PYR
BACTIDROP NINHYDRIN

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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