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: LRP FDA class 1

Tray, Surgical

General, Plastic Surgery

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The Surgical Tray is a prepackaged set of sterile surgical instruments and supplies assembled to facilitate various surgical procedures, providing a convenient and organized collection of tools for operating room use. It is classified as a Class 1 (lowest risk) device, subject only to general controls, representing the least burdensome regulatory category. The product code is LRP, regulated under 21 CFR 878.4800, within the General and Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

22 matches
K Number
Device Name
LACERATION TRAY
OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK
EYE TRAY
CUSTOM ENT PACKS
ORTHOPEDIC TRAY PRODUCT LINE
GENERAL SURGERY TRAY
HOSPITAL KIT ENT 1125
EYE TRAY
INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE
KITS AND TRAYS FOR ONE TIME USE ONLY
PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES
CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS
STERILE LACERATION TRAY
SITE STERILIZATION TRAYS FOR OPHTHALMIC USE
STERILE PACK (PROCEDURAL TRAY/KITS)
KOI(TM) INSTRUMENT TRAYS
SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
TODD MEDICAL/SKILLED CARE PRODUCTS
LACERATION AND INSTRUMENT TRAYS
LACERATION TRAY
MASTER KIT B
TRAY, SERVICE

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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