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: IYE FDA class 2

Accelerator, Linear, Medical

Radiology

View full classification →

A medical linear accelerator is a device used in radiation therapy to deliver high-energy X-ray or electron beams for the treatment of cancer and other tumors. It falls under FDA Class 2, indicating moderate risk; manufacturers must submit a 510(k) premarket notification demonstrating substantial equivalence to a legally marketed predicate device before marketing. The product code is IYE, regulated under 21 CFR 892.5050, within the Radiology medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
ThinkQA 3
LUNA 3D
AerFrame Patient Immobilization System (AFPIS)
VERIQA RT EPID 3D
ClearCheck (RADCC V2.7)
AlignRT Plus (8.0)
Halcyon, Ethos Radiotherapy System (5.0)
EMLA (Elekta Evo); EMLA (VersaHD); EMLA (Elekta Harmony Pro); EMLA (Elekta Infintiy); EMLA (Elekta Harmony); EMLA (Elekta Synergy)
ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface
ChartCheck (RADCH V1.6)
IDENTIFY (5.0)
ZAP-X Radiosurgery System (ZAP-X)
AccuCheck
MOSkin Radiation Measurement System
TrueBeam, TrueBeam STX, Edge and VitalBeam
AquaCast Mask
Cranial 4Pi Immobilization
MapRT
Mobius3D (4.1)
DSPS-Prominent® baseplate, MR (113820); DSPS-Prominent® baseplate (113120); DSPS-Prominent® Cradle-I (113140); DSPS-Prominent® Cradle-II (113150); DSPS-Prominent® Cradle-III (113160); DSPS-Prominent® Cradle-IV (113170); DSPS-Prominent® Cradle-VI (113180); DSPS-Prominent® Cradle-VII (113260); Mask DSPS®-PROSCVRL set/5 (113760); Mask DSPS®-PROSC set/5 (113770); Mask DSPS®-PROSCVR set/5 (113780); Mask DSPS®-PROSCL set/5 (113790); Mask DSPS®-PROSHVRL set/5 (113890); Mask DSPS®-PROSH set
Klarity SGRT System (ARSG-E1A, ARSG-E3A)
Identify (4.0)
ExacTrac Dynamic (2.0); ExacTrac Dynamic Surface
BeamDose software (S080053); BEAMSCAN software, option reference dosimetry (S080054.002)
Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)
VenusX
AlignRT Plus
LUNA 3D
ThinkQA (Edition 2)
Delta4 Insight
ArcherQA (V1.0)
kallisio stentra™ oral stent
TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)
BinkieRT
Halcyon, Ethos Radiotherapy System
TrueBeam, TrueBeam STx, Edge, VitalBeam
IDENTIFY
AccuCheck
Radixact Treatment Delivery System
MapRT
SIDDHARTH-II;IMPACT
TrueBeam, TrueBeam STx, Edge, VitalBeam
ExacTrac Dynamic 1.1.2
ARIA Radiation Therapy Management (v18.0)
Iris AirShuttle™
MOSAIQ® OIS (Oncology Information System)
Elekta Unity
DSPS-Prominent™ Masks; DSPS-Prominent™ Baseplate, MR; CouchStrip
Halcyon, Ethos Radiotherapy System
Klarity SRS Baseplate, Klarity Promise Baseplate

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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