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: DQC FDA class 1

Phonocardiograph

Cardiovascular

View full classification →

The Phonocardiograph is a cardiovascular diagnostic instrument used to record heart sounds and murmurs as a graphical waveform, aiding clinicians in the assessment of cardiac function and valvular conditions. It is classified as an FDA Class 1 device, representing the lowest level of regulatory concern, and is subject to general controls only. The product code is DQC and it is regulated under 21 CFR 870.2390 within the Cardiovascular medical specialty.

510(k) Clearances

18 matches
K Number
Device Name
CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH
LIFE SOUND SENSOR
ACOUSTIC RECORDER
PHONOCARDIOGRAPH
DYNAMIC SPECTRAL PHONOCARDIOGRAPH
ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE
PAG MICROPROCESSOR-CONTROLLED MODULE
MODIFIED DSP100 AMPLIFIER
ANDRIES PHYSICAL ASSESSMENT COMPUTER
DSP100 CAROTID PHONOANGIOGRAPHY MODULE
DSP100 AMPLIFIER
NON-INVASIVE CLINICAL VASCULAR LAB
MEDDARS/ULTRA IMAGER PULSE/PHON MODULE
MODEL 100 SPECTRAVIEW
NIC-200 VENTRICULAR FUNCTION ANALYZER
AMPLIFIER, PC-700
PULSE/PHONOCARDIOGRAPHY CHANNEL, 144
PHON/STRESS SYSTEM (#21126A)

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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