Therac 25

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K922276 ↗

FDA Product Code

IYE

Device Class

Class II

Regulation

21 CFR Part 892.5050

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Theraplan V05B/ Tp-11 V09B

  Class II

  FDA 510(k) K940237 Active Cleared 26 Jul 1994

• Theraton 1000E

  Class II

  FDA 510(k) K964607 Active Cleared 28 May 1997

• Theratron 780E

  Class II

  FDA 510(k) K964606 Active Cleared 26 Jun 1997

• Theratron 1000

  Class II

  FDA 510(k) K894165 Active Cleared 1 Feb 1990

• Theratronic Stimulator

  Class II

  FDA 510(k) K820782 Active Cleared 3 Jun 1982

• Theraplan Plus Version 1.2

  Class II

  FDA 510(k) K970236 Active Cleared 9 Jul 1997

See all devices from Theratronics, Inc. →