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: OBB FDA class 2

Kit, Conception-Assist, Home Use

Obstetrics/Gynecology

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The Kit, Conception-Assist, Home Use (product code OBB) is a home-use kit intended to assist conception in situations involving low sperm count, sperm immobility, or hostile vaginal environment, comprising cervical caps for semen collection and placement, polyurethane condoms, ovulation predictors, pregnancy tests, lubricant samples, and instructional materials, intended for use at home following physician instruction. It is classified as FDA Class 2, requiring 510(k) clearance, and is regulated under 21 CFR 884.5250 within the Obstetrics/Gynecology specialty. The device carries no implant or life-sustaining flags.

510(k) Clearances

4 matches
K Number
Device Name
THE STORK OTC
FOCUS TOUCH CONCEPTION SYSTEM
CONCEIVEX LATEX-FREE SEMEN COLLECTOR
CONCEIVEX CONCEPTION KIT

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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