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: JOP FDA class 2

Transducer, Ultrasonic

Cardiovascular

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The Transducer, Ultrasonic is a cardiovascular diagnostic device that converts electrical energy into ultrasonic waves and detects returning echoes to generate images or measurements of cardiac and vascular structures, used in echocardiography and Doppler flow studies for the noninvasive assessment of heart and vessel function. This device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification before marketing. It carries product code JOP and is regulated under 21 CFR 870.2880, within the Cardiovascular medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Falcon/Xpress (Falcon/Xpress)
VasoGuard (V10, V8, V6, V4, V2)
Smartdop XT6
SMARTDOP XT
VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDING
FALCON
STUDIODOP VICORDER
ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1
NICOLET VASOGUARD
ECHOFLOW DOPPLER BLOOD VELOCITY METER
SPECTRADOP
REUSABLE CW DOPPLER PROBES: MODELS P8M05S8A, P8M05N5A, & LCW-8
MODEL HD-207 BIDIRECTIONAL VELOCITY METER
EXTRAVASCULAR DOPPLER (EVD) ULTRA BLOOD FLOW PROBE
INTRAVASCULAR IMAGING SYSTEM/MODIFIED
FLOSCOPE VASCULAR LAB.
UST-2266U-5 CW DOPPLER TRANSDUCER
MILLAR MIKRO-TIP DOPPLER CATHETER
VOLUME COMPUTATION SOFTWARE PACKAGE
CARDIAC COMPUTATION SOFTWARE PACKAGE
INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515
RESUBMITTAL OF MI 1000C MICROIMAGER
TRANSESOPHAGEAL ECHO TRANSDUCER
SDU-700 PHASED ARRAY SECTOR AND LINEAR SCANNER
GENESIS II 7.5MHZ ULTRASOUND TRANSDUCER
BIOSOUND MMI ULTRASOUND
DOPPLEX ULTRASONIC DOPPLER SYSTEM
ABCOM 1 CARDIAC OUTPUT MONITOR
RT5000 ECHOCARDIOGRAPHY #H4100C/CE
MODIFIED RADIUS - MODEL NUMBER MM 5000
ACUSON L538 TRANSDUCER
AUXILIARY CONTINUOUS WAVE DOPPLER TRANSDUCER
MOD 482
5 MHZ TRANSDUCER
MASCOT CW DOPPLER SYSTEM
SSD-725 ULTRASOUND SECTOR SCANNER
CONTINUOUS CARDIAC OUTPUT MONITORING SYSTEM
SSD-633 PHASED ARRAY SECTOR/LINEAR ULTRASOUND SYS.
3MHZ ANNULAR ARRAY
CARDIOSCAN WITH DOPPLER OPTION
ACUSON L558 TRANSDUCER
ACUSON S519 TRANSDUCER
MERIDIAN IMAGING SYSTEM
ACUSON S319 TRANSDUCER
ACUSON L382 AND L312 TRANSDUCERS
ULTRAMED TF 122 ULTRASON VASCU IMAG & DOPPLER SYST
CARDIOSCAN DOPPLER OPTION
ULTRASOUND TRANSDUCER #21230A 7.5MHZ SHORT FOCUS
ULTRASONIC COUPLANT GEL
MERIDIAN ULTRASOUND IMAGING 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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