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: IWE FDA class 1

Monitor, Patient Position, Light-Beam

Radiology

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A light-beam patient position monitor is a non-ionizing optical device used in radiation therapy to verify and display the patient's position relative to the treatment field using a projected light beam, aiding accurate setup before radiation delivery. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IWE, regulated under 21 CFR 892.5780, within the Radiology medical specialty.

510(k) Clearances

28 matches
K Number
Device Name
CT Sim Laser System
DUAL RADIATION TARGETING SYSTEM DRTS DRAPE
GREEN TEC-2100
CENTRALITE BACKPOINTER
TEC-2110 GREEN LASER MODEL MT-HNG
CENTRALITE(R)-DLL SERIES
MED-TEC STRING RETICLE TRAY
HP BACK POINTER SYSTEM
LASER ALIGNMENT TOOL
TEC 2101 (MODEL MT-HPLGD)
TEC 2100 (MODEL MT-LPLGD)
RADIATION EXIT VERIFICATION SYSTEM/BACK POINTER SYSTEM
AZ 92
PATPOS GREEN
PATPOS COMPACT
PATPOS RED
ACCULITE SSL
A2J TELEMETER
DIOLASE
CENTRALITE BACKPOINTER
A2J MZ 44 B TYPE
ACCULITE
A2J MZ 44 LASER LIGHT FOR POSITIONING
CENTRALITE
NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESS
WALL MOUNTED LASER POSITIONING DEVICE
LASER BACKPOINTER ASSEMBLY, MOD. 01-2487
PATIENT POSITIONING SYSTEM 1D OR 2D

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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