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: QYW FDA class 2

Hospital Cardiac Telemetry

Cardiovascular

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The hospital cardiac telemetry device (product code QYW) is a Class 2 Cardiovascular prescription device (regulation 870.1025) intended to continuously record, display, and/or analyze electrocardiograms of patients in healthcare facilities for detecting conditions requiring prompt intervention, including automated detection of life-threatening arrhythmias and alarm generation with remote access capability. Requiring 510(k) clearance, it is intended for patients at elevated risk of serious cardiovascular events requiring prompt intervention and is staffed by onsite qualified personnel. It is designated as life-sustaining and is not an implant.

510(k) Clearances

2 matches
K Number
Device Name
TEMPUS PRO WITH ENHANCED FEATURES
HEARTRAC ECG MONITORING 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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