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: JSD FDA class 1

Culture Media, Selective Broth

Microbiology

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The Culture Media, Selective Broth is a microbiology diagnostic liquid medium that contains inhibitory agents to suppress the growth of unwanted organisms while allowing target organisms to proliferate, used in clinical laboratories to enrich and recover specific pathogens from specimens containing mixed microbial populations. This device is FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. It carries product code JSD and is regulated under 21 CFR 866.2360, within the Microbiology medical specialty.

510(k) Clearances

26 matches
K Number
Device Name
FASTIDIOUS INOCULUM BROTH
CAMPY BROTH
SABOURAUD DEXTROSE (SD) BROTH TUBE, #T3331
BRAIN HEART INFUSION BROTH W/6.5% NAC1 - #T3802
ALKALINE PEPTONE WATER
TODD HEWITT W/CNA (LIM BROTH)
T9802 TSB W/6.5% NACL
APL TRYPTIC SOY BROTH
TRYPTIC SOY BROTH W/6.5%SODIUM CHLORIDE
SELECTIVE CULTURE MED. TRICHOMONAS
SELECTIVE CULTURE MEDIUM
SELECTIVE BROTH
SF BROTH
SELENITE BROTH
GROUP STREP BROTH T3472 LIM
ROGOSA BROTH
BACTEC DILUTING FLUID
DERMATOPHYTE TEST MEDIUM
CULTURE MEDIA SELECTIVE BROTH
SELENITE BROTH
CAMPY THIOGLYCOLLATE (TUBE)
SABOURAUD LIQUID, BROTH MODIFIED
G N BROTH HAJNA
SELENITE BROTH
SELENITE CYSTINE BROTH
LAURYL TRYPTOSE BROTH

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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