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: KPY FDA class 1

Shield, Protective, Personnel

Radiology

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This device is a protective personnel shield, such as a lead apron or barrier, used by healthcare workers to reduce occupational radiation exposure during diagnostic or therapeutic radiological procedures. It is classified as FDA Class 1, the lowest risk category, subject to general controls only. The product code is KPY, regulated under 21 CFR 892.6500 within the Radiology specialty. No special flags apply.

510(k) Clearances

25 matches
K Number
Device Name
DISPOSABLE THYROID COLLAR
INTRA-ORAL THERMOPLASTIC SHIELD
THERMOPLASTIC SHIELD
UTK-DTE AUTILARY SHIELD
AUKULYTE
2001 SPECIAL PROCEDURE LAMP (LOW VOLTAGE) (AS EXHIBITS #2 & 4)
KENEX RADIATION SHIELD (VARIOUS MODELS AS EXHIBITS #2 & 5)
STAND IMAGING DOSE CALIBRATOR SHIELDED WORK PLATFORM
MAVIG ANGIO SHIELD MODELS 6290 & 6272
DAVIS LEAD APRON/RADIOGRAPHIC VARIOUS CAT. NUMBERS
DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS
DAVIS LEAD APRON GONADAL SHIELD-VARIOUS CAT. NOS.
RADIATION PROTECTION GLASSES
DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL
RADIATION PROTECTION APRON
PERSONNEL PROTECTIVE SHIELD
VENTIBOX
KRYPTON CART
BYPASS COIL
MOTI APRON
MOTI PROTECTIVE X-RAY MASK
FLOW MEDICAL X-RAY PROTECTIVE GLOVES
GONAD SHIELD
APRON, LEADED VINYL
GLOVE, SUPERFLEX MOLDED

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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