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: PRH FDA class 2

Positive Blood Culture Identification And Ast Kit

Microbiology

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The Positive Blood Culture Identification and AST Kit is an in vitro diagnostic kit using fluorescence in situ hybridization (FISH) for simultaneous identification and quantitative antimicrobial susceptibility testing (AST) of multiple microbial targets directly from positive blood culture specimens. It is classified as FDA Class 2 under 21 CFR 866.1650 in the Microbiology specialty, requiring 510(k) premarket notification. The device aids in rapid pathogen identification and guides antibiotic therapy selection. Product code PRH; not an implant and not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
Accelerate Pheno System, Accelerate PhenoTest BC Kit
Accelerate Pheno system, Accelerate Phenotest BC Kit

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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