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: SBO FDA class 1

Bed-Patient Activity Monitoring System

General Hospital

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A bed-patient activity monitoring system is a General Hospital device intended to monitor patient activity while lying in bed using pressure sensors placed on multiple body locations or under the mattress, with optional alarms to indicate when patient activity deviates from assigned pressure prevention parameters, helping prevent pressure injuries. It is classified as FDA Class I (general controls) under regulation 880.2400 in the General Hospital specialty, with product code SBO, and does not require 510(k) premarket notification. The device is not an implant and does not support life-sustaining functions.

510(k) Clearances

1 matches
K Number
Device Name
PRESSUREALERT® Pressure 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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