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.

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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: JSH FDA class 1

Culture Media, Non-Selective And Differential

Microbiology

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The Culture Media, Non-Selective and Differential is a microbiology diagnostic medium that supports the growth of a wide variety of microorganisms but contains indicators or reagents that produce visible differences in colony morphology or color based on the organisms' metabolic properties, enabling differentiation of colony types without inhibiting growth. This device is FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. It carries product code JSH and is regulated under 21 CFR 866.2320, within the Microbiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
FLO AGAR
UREA AGAR BASE
UREA BROTH
DNASE TEST AGAR
RUSSELL DOUBLE SUGAR AGAR
PHENOL RED BROTH BASE
MOELLERS DECARBOXYLASE, BASE
OF MEDIUM BASE
ACTINOMYCETE DIFFERENTIAL MEDIA
MAINTENANCE & CARBOHYDRATE FERMENTATION MEDIA
SIMMONS CITRATE MEDIUM SLANT, PRODUCT #T3084
MOTILITY INDOLE ORNATHINE (MIO) PRODUCT #T3053
LYSINE IRON AGAR (LIA) PRODUCT #T3046
IAFP MAC CONKEY AGAR
MUCATE AGAR, SLANTS AND MUCATE BROTH
SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM
ARYLSULFATASE BROTH
HEMOPHILUS ID QUAD PLATE
BIGGY AGAR
CLED AGAR
CLED AGAR WITH ANDRADES INDICATOR
THERMOSTABLE NUCLEASE TEST AGAR
THERMONUCLEASE AGAR W/TOLUIDINE BLUE
TRYCOPHYTON AGARS
STARCH AGAR W/BROM CRESOL PURPLE
XANTHINE/TYROSINE/CASEIN AGAR
MOTILITY INDOLE LYSINE SULFIDE (MILS) MEDIUM
BIRD SEED AGAR
TOC (TWEEN 80 - OXGALL-CAFFEIC ACID) AGAR
BIOTIS DECARBOXYLASE MEDIA, BASE
BIOTIS HAEMOPHILUS IDENTIFICATION QUAD
PSEUDOMONAS AGAR P (MEDIUM A)
APL MOTILITY INDOLE ORNITHINE AGAR
APL SIM MEDIUM
APL TRIPLE SUGAR IRON AGAR
APL FLUID THIOGLYCOLLATE MEDIUM
APL BILE ESCULIN/AZIDE AGAR
APL GN BROTH
APL DNASE TEST AGAR
APL CHLAMYDOSPORE AGAR
DNASE W/TOLUIDINE BLUE, DNASE W/INDICATOR
CLED AGAR
DRI-FORM PSEUDOMONAS AGAR F
TRIPLE SUGAR IRON AGAR
SIMMONS CITRATE AGAR
SIM MEDIUM
BIGGY AGAR NICKERSONS MEDIUM
UREA AGAR
OXIDATIVE FORMENTIVE MEDIUM
BROM CRESOL PURPLE STARCH

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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