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Delivery Analysis 1062213

by Accuray Incorporated

Delivery Analysis 1062213 is a Class II device made by Accuray Incorporated, cleared under FDA 510(k) K143269 on 14 Apr 2015 and listed in FDA GUDID since 11 Feb 2020 (UDI-DI M65810622130), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K143269

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM65810622130 UDI-DI Date11 Feb 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK143269 Date14 Apr 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K143269 decided 14 Apr 2015 Active
  • FDA GUDID UDI-DI M65810622130 listed 11 Feb 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K143269
  2. Listed FDA GUDID M65810622130

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Delivery Analysis
Generic name
Linear accelerator system
Model / Ref / Catalog
1062213
Primary DI / UDI-DI
M65810622130
510(k) Number
FDA product code
MUJ, IYE
GMDN term
Linear accelerator system
Device class
Class II
Regulation number
892.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Linear accelerator system

Cleared under the same submission (K143269)

Other devices from Accuray Incorporated

See all devices from Accuray Incorporated →

Properties

  • Prescription use
Other properties (14, all answered No)