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: JSI FDA class 1

Culture Media, Selective And Differential

Microbiology

View full classification →

The Culture Media, Selective and Differential is a microbiology diagnostic medium that both inhibits unwanted organisms and produces distinguishing reactions among organisms that do grow, enabling targeted recovery and presumptive identification of specific pathogens from complex clinical specimens in a single step. This device is FDA Class 1, the lowest risk category, requiring only general controls and no premarket notification. It carries product code JSI and is regulated under 21 CFR 866.2360, within the Microbiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
BBL CHROMAGAR 0157
DIPSTREAK
LISTERIA SELECTIVE ENRICHMENT MEDIUM
DENTOCULT SM-STRIP MUTANS
SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326
XL AGAR BASE
SELECTIVE STREPTOCOCCUS AGAR
TRICHOMONAS BROTH
TINSDALE AGAR BASE
MODIFIED SELECTIVE STREPTOCOCCUS AGAR
SELENITE BROTH
LOWENSTEIN-JENSEN, SELECTIVE
CORN MEAL W/POLYSORBATE 80
ATS MEDIA
DERMATOPHYTE TEST MEDIUM
QUAD PLATE (4 DIFFERENT MEDIA)
CORYNEBACTERIA ISOLATION MEDIA
SPECIALTY MEDIA
STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIA
MYCOLOGICAL MEDIA
MEDIA FOR DETECTION & VERIFICATION OF COLIFORMS
ENTERIC ISOLATION MEDIA
DIFFERENTIAL MEDIA
MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION
HEKTOEN ENTERIC (HE) AGAR/XLD AGAR BIPLATE #Z3016
HEKTOEN ENTERIC (HE) AGAR PRODUCT #P3330
LEVINE EOSIN METHYLENE BLUE AGAR (LEMB) - #P1507
EOSIN METHYLENE BLUE AGAR (EMB) - PRODUCT #P1309
XYLOSE LYSINE DEOXYCHOLATE AGAR - PRODUCT #P3601
MANNITOL SALT AGAR (MSA) PRODUCT #P1706
MACCONKEY AGAR - PRODUCT #P1606
DENTOCULT-SM CULTURE-PADDLE
MACCONKEY AGAR - PRODUCT #P1606
IAFP BILE ESCULIN AZIDE AGAR
IAFP X.L.D. AGAR
IAFP MANNITOL NACL
IAFP BILE ESCULIN AGAR
IAFP S.S. AGAR
SORBITOL MACCONKEY AGAR NO. 3 CM 813
MACCONKEY W/SORBITOL
ORICULT-N CULTURE-PADDLE
BACTEROIDES BILE ESCULIN AGAR
STAPHYLOCOCCUS 110 AGAR
CETRIMIDE SELECTIVE AGAR
BRILLIANT GREEN AGAR
POTATO DEXTROSE AGAR
BRILLIANT GREEN AGAR
ANAEROBIC LKV BLOOD AGAR
MACCONKEY AGAR
HEKTOEN ENTERIC AGAR

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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