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: MYF FDA class 2

Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2

Microbiology

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The Enzyme Linked Immunosorbent Assay (ELISA) for Herpes Simplex Virus Type 2 (HSV-2) is an in vitro diagnostic test used to detect antibodies against HSV-2 in patient serum or plasma, supporting the serological diagnosis and type-specific differentiation of genital herpes. Classified as FDA Class 2, it requires 510(k) premarket clearance under regulation 866.3305 (Microbiology specialty).

510(k) Clearances

10 matches
K Number
Device Name
ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls
Elecsys HSV-2 IgG (08948887160)
SeraQuest HSV Type 2 Specific IgG
ADVIA Centaur Herpes-2 IgG
SeraQuest HSV Type 2 Specific IgG
ZEUS ELISA HSV GG-2 IGG TEST SYSTEM
LIAISON HSV-2 TYPE SPECIFIC IGG ASSAY, CONTROL HSV-2 IGG
EUROIMMUN ANTI-HSV-2 ELISA (IGG) AND ANTI-HSV-1 ELISA (IGG) KIT
CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT
HSV-2 ELISA IGG, MODEL EL0920G

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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