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: KZM FDA class 2

Device, Muscle Monitoring

Physical Medicine

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The Muscle Monitoring Device is a diagnostic instrument used in physical medicine and rehabilitation settings to assess muscle activity, tone, or contractile function, providing clinicians with objective data to guide treatment planning and monitor patient progress. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification before marketing. The product code is KZM, regulated under 21 CFR 890.1375, in the Physical Medicine medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

19 matches
K Number
Device Name
TEETHAN 2.0
M-SCAN
GRINDCARE MEASURE
BIOEMG III
DOLOTENS DENTAL TM 1
BITESTRIP
BIOEMG II AND BIOJVA
MODEL K7 EVALUATION DEVICE
MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I
BIOPAK MEASUREMENT SYSTEM
K6-1 DIAGNOSTIC SYSTEM VERSION 3.1
K6-I DIAGNOSTIC SYSTEM
MS-100 MYO-SCANNER OR MS-100 EMG SCANNER
BIO-EMG MODEL 800
E.W.L. P-TENS/H-WAVE
COMFORTRON
DENTAL ANESTHESIA APPARATUS
MODEL EM-2 BIOELECTRIC PROCESSOR
MODEL EM-IR

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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