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: KNA FDA class 2

Instrument, Manual, Specialized Obstetric-Gynecologic

Obstetrics/Gynecology

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A Specialized Manual Obstetric-Gynecologic Instrument is a hand-held surgical tool designed for specific obstetric or gynecologic procedures such as cervical biopsy, endometrial sampling, or other specialized interventions in the care of female reproductive health. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket notification. The product code is KNA and it is regulated under 21 CFR 884.4530 in the Obstetrics and Gynecology specialty.

510(k) Clearances

50+ matches
K Number
Device Name
PANPAC WORD/BARTHOLIN CATHETER
COOK WORD BARTHOLIN GLAND CATHETER (FINAL TRADE NAME NOT YET DETERMINED)
GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETER
COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400
BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500
EPISTAT, V-STAT, MODELS EPISTAT-001-01, V-STAT-001-01
TAMPONADE UTERINE BALLOON CATHETER SET
DND 202 MANUAL UROLOGICAL DIGITAL NEEDLE DRIVER
DND 101
DR. JAHANGER'S CUTTER
BERACLAMP, MODEL BC-1
SCC-23 SAFETY CLAMP AND CUTTER
UROMED SLING KIT
GYNEX ENDOSPECULUM
NATIONAL MEDICAL HEALTHCARE CUSTOM OB/GYN KITS, TRAYS, OR PACKS
SAFE-T-CLAMP
BALLOON UTERINE STENT
CORDGUARD II
OB/GYN PACKS
MADDEN SURGICAL THIMBLE
DISPOSABLE EMERGENCY OBSTETRICAL KIT
ENDO CERVICAL CURETTE
NEEDLE EXTENSIONS
MICRO SURGERY SCISSORS
MICRO SURGERY NEEDLE HOLDERS
Z CLAMP SCISSORS
MIYA HOOK
VARIOUS SCISSORS
RETRACTOR RODS
C-SECTION TRAY
RETRACTOR RODS
CORSON MYOMA GRASPING FORCEPS
GREENE-ARMYTAGE HEMOSTATIC FORCEPS
MIYA HOOK
SOPHER AND BIERER OVUM FORCEPS
OVUM FORCEPS-BARRET,JAVERTS,WILLET,HANSEN,COREY,MC
MICRO SURGERY NEEDLE HOLDERS
MICRO SURGERY FORCEPS
MICRO SURGERY SCISSORS
COOK HYSTEROCATH(TM)
WORD BARTHOLIN GLAND CATHETER CODE: 1005
INTRAUTERINE HEMOSTASIS BALLOON STENT
MODIFIED HYSTEROSALPINGOGRAPY SET
OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KIT
MILEX BARTHOLIN GLAND CATHETER
MICROINFERTILITY NEEDLE HOLDER, TITANIUM
MICROINFERTILITY SCISSORS, TITANIUM
MICROINFERTILITY FORCEPS, TITANIUM
ACKRAD HYSTEROSALPINGOGRAPHY SET
OVARY FORCEPS

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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