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: HDD FDA class 2

Table, Obstetrical, Ac-Powered (And Accessories)

Obstetrics/Gynecology

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The AC-Powered Obstetrical Table and Accessories is an electrically powered patient positioning table designed for labor, delivery, and gynecological procedures, with adjustable sections and accessory attachments to support obstetrical care. It is classified as a Class 2 device (moderate risk). The product code is HDD under regulation 21 CFR 884.4900 in the Obstetrics/Gynecology specialty. No implant, life-sustaining, GMP exempt, or third-party review flags apply.

510(k) Clearances

7 matches
K Number
Device Name
ADEL 5000
THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES
ORCEPAD
ADEL MODEL 2100 BIRTHING BED
ADEL MEDICAL BIRTHING BED, #LD-500
TILT 10, CATALOG #S-2600
CART, PROCEDURES

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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