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: QBD FDA class 2

Microbial Nucleic Acid Storage And Stabilization Device

Microbiology

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The Microbial Nucleic Acid Storage and Stabilization Device (also described as molecular transport media) is intended for the stabilization and transportation of nucleic acids from unprocessed human samples suspected of containing infectious material, used to preserve specimen integrity during transport to a laboratory. It is classified as a Class 2 device under regulation 866.2950, requiring 510(k) premarket notification, and falls within the Microbiology (MI) medical specialty. The product code is QBD. It is not an implant and is not life-sustaining.

510(k) Clearances

17 matches
K Number
Device Name
Puritan PurSafe Plus Collection and Transport System
PPH Saliva Collection Kit
Sample Preservative Fluid
Molecular Transport Media - MTM
InActiv Blue
Sample preservation solution
DNA/RNA Shield SafeCollect Saliva Collection kit
CLEARinse CTS Specimen Collection and Transport System
iSWAB-Respiratory Tract Sample Collection Media-Extraction Less (iSWAB-RC-EL)
Spectrum Saliva Collection Device
Biosci™ Inactivated Transport Medium, Biosci™ ITM
Dasky Disposable Sampling Tube (Model name: VSM02)
MagXtract Collection Tube
Disposable Sampler Inactivated Transport Media, Nest ITM
DNA/RNA Shield Collection Tube
eNAT molecular collection and preservation medium
PrimeStore MTM

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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