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: PFA FDA class 2

Non-Invasive Central Venous Manometer

Cardiovascular

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The Non-Invasive Central Venous Manometer is a cardiovascular device that measures central venous blood pressure (CVP) non-invasively at the superior vena cava (right heart) based on near-infrared or related optical sensing technology, without the need for invasive catheter placement. It falls under the Cardiovascular medical specialty and is classified as a Class 2 device under regulation 870.1140, requiring 510(k) premarket notification. Non-invasive CVP measurement reduces the risks associated with central venous catheterization. It is not an implant and is not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
Central Venous Pressure System
CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000

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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