Tray Adapters, Multiple

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K010174 ↗

FDA Product Code

IYE

Device Class

Class II

Regulation

21 CFR Part 892.5050

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Intra Operative Radiation Therapy

  Class II

  FDA 510(k) K004023 Active Cleared 21 Sep 2001

• Breast-Board (Multiple)

  Class II

  FDA 510(k) K003778 Active Cleared 8 Jun 2001

• Styrofoam Cutters for Block Casting System

  Class II

  FDA 510(k) K010062 Active Cleared 13 Mar 2001

• Cranial Stereotactic Equipment

  Class II

  FDA 510(k) K010065 Active Cleared 2 Jul 2002

• Couch for Total Body Radiation

  Class II

  FDA 510(k) K010063 Active Cleared 2 Apr 2001

• Lead Blocks

  Class II

  FDA 510(k) K010172 Active Cleared 18 Apr 2001

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