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: KNC FDA class 2

Table, Obstetric (And Accessories)

Obstetrics/Gynecology

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An Obstetric Table with Accessories is a specialized examination and delivery table used in obstetrics and gynecology to position patients for labor, delivery, and gynecologic procedures, with adjustable components and accessories to support clinical care. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket clearance. The product code is KNC and it is regulated under 21 CFR 884.4900 in the Obstetrics and Gynecology specialty.

510(k) Clearances

26 matches
K Number
Device Name
L720 EXAMINATION CHAIR
NON-LINTING DELIVERY BLANKET
MEDICAL DISPOSABLE BEDDING
BD6000 THE OPTIMA & BD5000 BIRTHING BED
AFFINITY BED MODEL 3600 SERIES
GARDOSI BIRTHING CUSHION
OBSTETRICAL SAFETY SYSTEM
STRYKER MODEL 977 BIRTHING BED
PALMER OBSTETRIC BRACE
MERIVAARA OBSTETRIC CHAIR/BED-MODEL 358
LABOR-DELIVERY STRETCH/BED
MERIVAARA OBSTETRIC CHAIR/BED MODEL 358
CAT. NO. S-5300-E BIRTHING BED
PALMER OBSTETIC BRACE
LORRAINE DSL LABOR & DELIVERY BED
LABOR/DELIVERY/RECOVERY BED LDR-600
BIRTHWELL BIRTHING SYSTEM
DELIVERY 4 TABLE
S & W MODEL ASO
O.N.A.T.
CENTURY BIRTHING CHAIR
LIC OBSTETRICAL TABLE
ADEL MEDICAL BIRTHING BED, MOD. LD-400
OBSTETRICAL BEDS
S/A 7800 BIRTH SUPPORT CHAIR
TABLE, EXAMINATION

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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