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: HQR FDA class 2

Apparatus, Cautery, Radiofrequency, Ac-Powered

Ophthalmic

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An AC-Powered Radiofrequency Cautery Apparatus is a mains-powered ophthalmic surgical device that delivers radiofrequency electrical energy to tissues for controlled cauterization and hemostasis during ophthalmic and periocular surgical procedures, offering consistent and sustained power delivery compared to battery-powered units. This device is FDA Class 2 (moderate risk), requiring premarket notification (510(k)) before marketing. It carries product code HQR and is regulated under 21 CFR 886.4100, within the Ophthalmic medical specialty. It is eligible for third-party review.

510(k) Clearances

11 matches
K Number
Device Name
THERMAL CAUTERY PROBE
DI-RHEX OPHTHALMIC DIATHERMY SYSTEM
REFRACTEC MCS-100
PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)
STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)
SURGITRON
GAMP & ASSOCIATES THREE FUNCTION DISPOSABLE MANIPULATOR
RETURN PATH DIATHERMY HANDLE
MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATION
ADVANCED SURGICAL SOLID STATE BIPOLAR COAGULATOR
UNITED SURGICAL CORP. DIATHERMIC PLUS

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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