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: PAF FDA class 2

Voltage Gated Calcium Channel (Vgcc) Antibody Assay

Immunology

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The Voltage Gated Calcium Channel (VGCC) Antibody Assay is an immunology in vitro diagnostic device intended for the semi-quantitative determination of VGCC antibodies in human serum; VGCC antibodies may be present in patients diagnosed with Lambert-Eaton Myasthenic Syndrome (LEMS), and results are to be used in conjunction with other clinical, electrodiagnostic, and laboratory findings. It is classified as Class 2 (FDA Class 2), requiring 510(k) premarket clearance, and is eligible for third-party review. The product code is PAF, with regulation number 866.5660 under the Immunology medical specialty.

510(k) Clearances

1 matches
K Number
Device Name
KRONUS VOLTAGE GATED CALCIUM CHANNEL (VGCC) ANTIBODY RIA ASSAY 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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