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: MAA FDA class 2

Monitor, Fetal Doppler Ultrasound

Obstetrics/Gynecology

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The Fetal Doppler Ultrasound Monitor (product code MAA) is a diagnostic device that uses Doppler ultrasound technology to continuously monitor and display the fetal heart rate during pregnancy or labor, providing real-time assessment of fetal well-being. Regulated under 21 CFR 884.2660 and classified as a Class 2 device, it requires a 510(k) premarket notification and is eligible for third-party review. The device falls under the Obstetrics/Gynecology specialty with review by the Radiology (RA) panel. It is not an implant and is not life-sustaining.

510(k) Clearances

9 matches
K Number
Device Name
ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER
LIFEDOP MODEL, L350R
GE SONOCHROME
FETAL DOPPLER
L582 TRANSDUCER
L328 TRANSDUCER
S5192R TRANSDUCER
SONICAID MODEL VASOFLO 4
QUANTUM QAD ANGIODYNOGRAPH ULTRASOUND SYSTEM

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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