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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: QAQ FDA class 2

Adjunctive Predictive Cardiovascular Indicator

Cardiovascular

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The Adjunctive Predictive Cardiovascular Indicator is a prescription software device that uses algorithms to analyze cardiovascular vital signs and predict future cardiovascular status or events, intended for adjunctive use alongside other physical vital sign parameters and patient information, and not designed to independently direct therapy. It is classified as a Class 2 device under regulation 870.2210, requiring 510(k) premarket notification, and falls within the Cardiovascular (CV) medical specialty. The product code is QAQ. It is not an implant and is not life-sustaining.

510(k) Clearances

5 matches
K Number
Device Name
Hypertension Prediction Index (HePI) Algorithm
Acumen Hypotension Prediction Index (HPI) Algorithm
Acumen Hypotension Prediction Index, HemoSphere Advanced Monitoring Platform
Acumen Hypotension Prediction Index – EV1000 Clinical Platform, Acumen Hypotension Prediction Index – HemoSphere Advanced Monitoring Platform, Acumen Hypotension Prediction Index – HemoSphere Advanced Monitoring Platform - Pressure
Acumen Hypotension Prediction Index (HPI) Feature Software

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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