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: JSJ FDA class 1

Culture Media, Selective And Non-Differential

Microbiology

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The Culture Media, Selective and Non-Differential is a microbiology diagnostic medium that contains inhibitory agents to suppress non-target organisms while allowing target organisms to grow without producing distinguishing colony characteristics, used for recovery and enrichment of specific pathogens from clinical specimens without differentiation. This device is FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. It carries product code JSJ and is regulated under 21 CFR 866.2360, within the Microbiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421
MYCOLOGICAL AGAR W/LOW PH
BRILLIANT GREEN AGAR W/SULFADIAZINE
W-L DIFFERENTIAL MEDIUM
INHIBITORY MOLD AGAR
LITTMAN AGAR
YM BROTH
CHAPMAN STONE MEDIUM
SABOURAUD MALTOSE AGAR
MITIS SALIVARIUS AGAR
PHYTONE YEAST EXTRACT AGAR
DERMATOPHYTE TEST MEDIUM
TERGITOL 7 BROTH
STREPTOSEL
LOWENSTEIN-JENSEN, W/NACL
LOWENSTEIN-JENSEN SLANT
CAMPLYOBACTER CULTURE MEDIA PRODUCTS P3873/T3597
SABOURAUD DEXTROSE AGAR W/CHLORO
CETRIMIDE SELECTIVE AGAR
BCYE, SELECTIVE (W/MPA)
BCYE AGAR
BHI WITH C & C SLANT
SLIDE CULTURE PLATE-POTATO FLAKE AGAR
SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR
BIOTIS (TM) HAEMOPHILUS DUCREYI
BIOTIS (TM) BCYE SELECTIVE
TSA W/NEOMYCIN & 5% SHEEP BLOOD - # P3104 & Z3050
BIOTIS (TM) INHIBITORY MOLD AGAR (DOUBLE POUR)
BIOTIS (TM) BHI WITH HRBC, CHLORA/GENTAM/CYCLOHEXI
MICRO CULTURE MEDIA P3528, P3137, P3149, P3139
PHENYLETHYL ALCOHOL AGAR(PEA) W/5% SHEEP #P3323
COL. CNA 5% SB/MACCONKEY AGAR BIPLATE # Z3206
MYCOLOGY W/CYCLOHEXANIDE & CHLORAMPHEMICOL (C&C)
GRAM NEGATIVE (GN) BROTH, PRODUCT #T3038
SABOURAUD DEXTROSE (SD) AGAR, PRODUCT #P3330
SABOURAUD DEXTROSE (SD) AGAR SLANT TUBE #T3080
SABOURAUD DEXTROSE SD AGAR SLT TUBE W/C&C #T4412
SABOUR DEXTR W/CHLORAMPHEN/GENTAM SD W/C&G AGAR PL
SABOUR DEXTR SD AGAR SLNT TUBE W/CHLORAMP #T3088
SABOURAUD DEXTROSE (SD) W/CHLORAMP AGAR PLATE
BRAIN HEART INFUS AGAR SLANT W/10% SHEEP BLOOD C&C
BRAIN HEART INFUS AGAR W/5% SB & GENTAMICIN-#P3772
BRAIN HEART INFUS AGR SLT W/5% SHP BLD PENIC/STREP
BRAIN HEART INFUS AGAR SLANT W/6% SB CHLORAMPHENIC
BRAIN HEART INFUS AGAR W/5% SB & CHLORAMPHENICOL
BRAIN HEART INFUSION SELECTIVE AGAR SLANT - #T4463
BRAIN HEART INFUS AGAR W/5% SB PENICILLIN/STREPTOM
BRAIN HEART INFUSION AGAR SLANT/GENTAMICIN #T4450
BRAIN HEART INFUS AGAR SLT W/5% SHEEP BLOOD/GENTAM
BRAIN HEART INFUSION AGAR W/ C&C SLANT TUBE #T3285

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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