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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: JSF FDA class 1

Culture Media, Single Biochemical Test

Microbiology

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The Culture Media, Single Biochemical Test is a microbiology diagnostic medium designed to perform a single defined biochemical test reaction that detects a specific metabolic property of a microorganism, used to confirm the identity of bacterial isolates as part of routine clinical microbiology identification procedures. This device is FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. It carries product code JSF and is regulated under 21 CFR 866.2320, within the Microbiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
NUTRIENT GELATIN - PRODUCT NUMBER T2860
LAURYL TRYPTOSE BROTH
MOELLERS DECARBOXYLASE, ONITHINE
MOELLERS DECARBOXYLASE, LYSINE
CYSTINE TRYPTIC MEDIUM W/ MALTOSE
ACETAMIDE AGAR SLANT
ONPG TEST REAGENT
BRILLIANT GREEN BILE BROTH
NITRATE BROTH
MOELLOERS DECARBOXYLASE, ARGININE
CYSTINE TRYPTIC MEDIUM W/SUCROSE
CYSTINE TRYPTIC MEDIUM W/LACTOSE
CYSTINE TRYPTIC MEDIUM W/DEXTROSE
NUTRIENT GELATIN
BIOTIS (TM) STARCH HYDROLYSIS WITH BCP
BIOTIS (TM) MUELLER HINTON W/4% SALT, 6MCG/ML OXAC
CULTURE MEDIA T2995/2954/2992/2991/2993/2994/2990
IAFP UREA AGAR SLANT
TRYPTONE BROTH, 2%
DNASE AGAR
TRYPTONE WATER (1%)
BIOTIS DECARBOXYLASE MEDIA, LYSINE
BIOTIS MOTILITY TEST MEDIUM
BIOTIS DECARBOXYLASE MEDIA, ARGININE
BIOTIS DECARBOXYLASE MEDIA, ORNITHINE
CAFFEIC ACID DISK
SIMMONS CITRATE AGAR
ACETATE DIFFERENTIAL AGAR
CYSTINE TRYPTIC AGAR W/DEXTROSE
CYSTINE TRYPTIC AGAR W/LACTOSE
CYSTINE TRYPTIC AGAR W/MALTOSE
CYSTINE TRYPTIC AGAR W/MANNITOL
CYSTINE TRYPTIC AGAR W/SUCROSE
CYSTINE TRYPTIC AGAR W/FRUCTOSE
PHENOL RED BROTH W/CARBOHYDRATES
DIFFERENTIATION DISKS BILE ESCULIN
HIPPURATE TEST REAGENT
DECARBOXYLASE TEST REAGENT
VOGES-PROSKAUER REAGENT A
CHRISTENSEN'S UREA AGAR
HIPPURATE TEST DISKS
INDOLE REAGENT
LYSINE IRON AGAR
VOGES-PROSKAUER REAGENT B
STREP-A-CHEK
ZINC DUST SUSPENSION
OXIDASE TEST STRIPS-OXIDASESURE
ARGINIE BROTH
ONPG DISKS
SPOT TEST NINHYDRIN REAGENTS

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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