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: JOS FDA class 2

Electrode, Electrosurgical

General, Plastic Surgery

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The Electrode, Electrosurgical is a surgical device used in electrosurgical procedures to deliver radiofrequency electrical current to tissue for cutting, coagulation, or ablation during general and plastic surgery operations, functioning as the active component through which current passes to the patient. This device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification prior to marketing. It carries product code JOS and is regulated under 21 CFR 878.4400, within the General, Plastic Surgery medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

36 matches
K Number
Device Name
Resection Electrodes
LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR
REPROCESSED ELECTROSURGICAL ELECTRODE
MEDLINE GROUNDING PAD
ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999
STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD
ULTRABLATOR ELECTRODE
CAPSULAR SHRINKAGE ELECTRODE
STANDARD AND EXTENDED BLADE, NEEDLE AND BALL; MODIFIED STANDARD AND EXTENDED BLADE & NEEDLE; STANDARD 45 DEGREE BLADE
VALLEY FORGE BIPOLAR BALL TIP ELECTRODE
STANDARD & EXTENDED BLADE/NEEDLE/BALL;MODIFIED STANDARD & EXTENDED BLADE/NEEDLE
MICRO DIAMOND-POINT DISSECTION NEEDLES
MODIFIED LEVEEN NEEDLE ELECTRODE
SENTRY DISPOSABLE DISPERSIVE ELECTRODE
MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES, SURGICAL INSTRUMENTS USED DURING ENDOSCOPIC PROCEDURES
MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES
DEVICE, ELECTROSURGICAL, CUTTING AND COAGULATION & ACCESSORIES
ELECTRODES
MILES SODIUM METHOD
ELECTRODE EXTENDER
ELECTRODE, ELECTROSURGERY
ELECTROSURGICAL ELECTRODE
MICRO CAUTERY NEEDLES
HOOK TIP SURGICAL CAUTERY ELECTRODE BLADE
STRAIGHT PADDLE SURGICAL CAUTERY ELECTRODE BLADE
INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE
COLORADO NEEDLE ELECTRODE
YESNG PATIENT PLATE #80226
STRATUM ESU
MONOPOLAR CAUTERY RETROGADE TIP #TM-1703
MONOPOLAR CAUTERY BLADE TIP #TM-1701
MONOPOLAR CAUTERY CONICAL TIP #TM-1702
ELECTROSURGICAL CUTTING & COAGULATION
BIPOLAR FORCEPS
INFANT ELECTROSURGICAL GROUNDING PAD
ELECTROSURGICAL GROUNDING PAD

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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