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: BWK FDA unclassified

Stimulator, Electro-Acupuncture

Unknown

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The Stimulator, Electro-Acupuncture is a device that delivers low-level electrical current through acupuncture needles to stimulate acupuncture points, used as a treatment in pain management and other therapeutic applications. Its FDA device class is currently unclassified; the device has not yet been formally categorized into Class 1, 2, or 3 and is awaiting classification action. The product code is BWK, with no assigned regulation number, reviewed by the Neurology panel.

510(k) Clearances

23 matches
K Number
Device Name
Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)
Needle Stimulator (Model: RJNS6-1)
Needle Stimulator
AXUS ES-5 Electro-Acupuncture Device
ANSiStim-PP
Stivax
ANSISTIM
PANTHEON ELECTROSTIMULATOR
Electro Auricular Device
P-STIM
JIAJIAN CMN STIMULATOR
JIAJIAN ELECTRO-ACUPUNCTURE STIMULATORS
MULTI-PURPOSE HEALTH DEVICE
ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01
E-PULSE
MODEL ES-130
P-STIM SYSTEM
ACULIFE, MODEL SMW-01
ACUSTIM
PULSELIFE STIMULATOR
ACUPUNCTURE INSOLES
SELECTRODE SYSTEM
HEALTH POINT

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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