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: JSL FDA class 1

Culture Media, Anaerobic Transport

Microbiology

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The Culture Media, Anaerobic Transport is a microbiology diagnostic transport medium designed to maintain the viability of obligate and facultative anaerobic microorganisms in clinical specimens during transport from the collection site to the laboratory, preserving organisms that would otherwise be inactivated by oxygen exposure before culture can be initiated. This device is FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. It carries product code JSL and is regulated under 21 CFR 866.2390, within the Microbiology medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

8 matches
K Number
Device Name
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITHOUT CHARCOAL
KULTSURE/STARSWAB ANAEROBIC TRANSPORT SYSTEM
BIONOR TRANSPORTMEDIUM
ANAEROBIC TRANSPORT MEDIUM
ANA TRANS TUBE & SWABS STERILE PACK
PRE-REDUCED ANAEROBIC MEDIA
PRE-DUCED CULTURE MEDIA

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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