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: PHU FDA unclassified

Intra-Abdominal Pressure Monitoring Device

Unknown

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The Intra-Abdominal Pressure Monitoring Device is used for monitoring abdominal intracompartmental pressure, typically using bladder pressure as a surrogate measure for intra-abdominal pressure in critically ill patients. It is classified as "Unclassified" (Class U) by the FDA, having received 510(k) clearance without formal class assignment, reviewed by the General and Plastic Surgery (SU) panel. The product code is PHU, and it is flagged as an implant given that it involves intrabody pressure measurement via an indwelling catheter. No regulation number or medical specialty is assigned.

510(k) Clearances

2 matches
K Number
Device Name
TraumaGuard Intra-abdominal Pressure Sensing System
BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001

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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