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: BXN FDA class 2

Stimulator, Nerve, Battery-Powered

Anesthesiology

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The Stimulator, Nerve, Battery-Powered is a portable, battery-operated device that delivers controlled electrical pulses to peripheral nerves for nerve localization during regional anesthesia or monitoring of neuromuscular blockade. It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is BXN, regulated under 21 CFR 868.2775 in the Anesthesiology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
STIMPOD NMS450 Nerve Stimulator
MultiStim ECO
SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator
MiniStim MS-IVB Peripheral Nerve Stimulator
STIMPOD ST2-3010 NERVE STIMULATOR
EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN
MYOGUIDE SYSTEM MODEL 8008
STIMTRODE SINGLE USE NERVE STIMULATOR
STIMPOD NMS450 NERVE STIMULATOR
STIMPOD MODEL NMS-400 NERVE STIMULATOR
ASCEND
XPOD/XMAP NERVE STIMULATOR
MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098
CLAVIS
STIMUPLEX PEN
PAJUNK MULTISTIM SENSOR NERVE STIMULATORS
STIMUPLEX HNS-12, MODEL 4892098
STIMUPLEX-DIG-RC NERVE STIMULATOR
MULTISTIM
TE ME NA POLYSTIM NERVE STIMILATOR
STIMUPLEX HNS-11
SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
VITALMAX 840 SERIES
MS-III MINISTIM
NEUROMUSCULAR TRANSMISSION MONITOR
MYOTRACK, MODEL HH 515
MODIFIED AXOSTIM
MINI ACCELOGRAPH NEUROMUSCULAR TRANS. MONITOR
BIO-INDUSTRY STIM POCHE(R)
ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR
MYOTEST DBS NERVE STIMULATOR
AXOSTIM
MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM
TRACER
CONSTANT CURRENT PERIPHERAL NERVE STIM. #NS252
ACCELOGRAPH
MODEL MS-II MINISTIM
MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT
TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCK
MODIFIED NEUROMUSCULAR TRANSMISSION MONITOR
MODEL 100 NERVE STIMULATOR
MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING
MYOTEST - NERVE STIMULATOR
STIMUPLEX, NERVE STIMULATOR
THE GRIPPER
T4 MONITOR STIMULATOR COMPUTER
NERVE FINDER
MEDAR APM FORCE TRANSDUCER
PERIPHERAL NERVE STIMULATOR MODEL A400
NERVE STIMULATOR Q10

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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