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.

Product Code: FAQ FDA class 1

Bag, Urine Collection, Leg, For External Use, Sterile

Gastroenterology, Urology

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The Sterile Leg Urine Collection Bag for External Use (product code FAQ) is a wearable urine collection bag secured to the leg, intended for patients who require external urinary drainage without an indwelling catheter. It is an FDA Class 1 device (lowest risk), subject only to general controls with no premarket notification required. It is regulated under 21 CFR 876.5250 in the Gastroenterology and Urology specialty. No special flags apply.

510(k) Clearances

18 matches
K Number
Device Name
PROSYS CUSTOM FIT LEG BAG WITH PREATTACHED ADJUSTABLE INLET TUBE FOR PATIENT SIZING
CPR URINE BAG
CONVEEN URINE BAG - STERILE
PROSYS BEDSIDE DRAINAGE BAG
CONVEEN LEG BAG STRAP
PROSYS LEG BAG
URINE COLLECTOR & ACCESSORIES
ALPINE REUSABLE LEG BAGS
URINARY DRAINAGE BAG CADDY
BARD LEG BAG HOLDER
CONVEEN(R) LEG BAG(500 ML)
ILC LEG BAG HOLDER
EXTERNAL LEG BAG
URINARY LEG BAG
4 SURE URINARY LEG BAG
CATHETER STRAP & RUINARY BAY HOLDER
QUADRIPLEGIC URINARY DRAINAGE VALVE
URINARY LEG BAG

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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