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Delivery Analysis

FDA UDI

Class II (US FDA UDI)

by Accuray Incorporated

Identity

Trade Name
Delivery Analysis FDA UDI
Generic Name
Linear accelerator system FDA UDI
Device Name
Software, Delivery Analysis, Version 1.2.2 FDA UDI
Model / Reference
1064315 FDA UDI
Description
Software, Delivery Analysis, Version 1.2.2 FDA UDI

Identifiers

Catalog Number
NA FDA UDI
Primary DI / UDI-DI
M65810643150 FDA UDI
510(k) Number
K143269 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Linear accelerator system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Linear accelerator system

Delivery Analysis by Accuray Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Linear accelerator system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c8ecd0f0-fdaf-438d-8741-7c61f3e8f16a 36 fields · synced Jun 9, 2026