MRT-150 QD Knee Coil

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

510(k) Number

K920096 ↗

FDA Product Code

LNH

Device Class

Class II

Regulation

21 CFR Part 892.1000

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Opart, Model Mrt-600

  Class II

  FDA 510(k) K991740 Active Cleared 2 Aug 1999

• Mrt 50A Flexible Body Coil

  Class II

  FDA 510(k) K900285 Active Cleared 9 Mar 1990

• Mrt-50

  Class II

  FDA 510(k) K921413 Active Cleared 14 Aug 1992

• Flexart V3.5 Software

  Class II

  FDA 510(k) K970573 Active Cleared 21 Jul 1997

• Mrt 50A Joint Coil

  Class II

  FDA 510(k) K900727 Active Cleared 9 Mar 1990

• Mrt 50A

  Class II

  FDA 510(k) K903770 Active Cleared 20 Nov 1990

See all devices from Toshiba America Mri, Inc. →

• What is the MRT-150 QD Knee Coil used for?

  The MRT-150 QD Knee Coil is designed for Nuclear Magnetic Resonance Imaging specifically of the knee area when used with compatible MRI systems in radiology settings.

• How is the MRT-150 QD Knee Coil supplied?

  The device is supplied by Toshiba America MRI, Inc. and is intended for use in radiology settings as a Class II medical device.

• What is the regulatory status of the MRT-150 QD Knee Coil?

  The device is authorized under FDA 510K clearance with product code LNH and regulation number 892.1000, classified as substantially equivalent.

• Is the MRT-150 QD Knee Coil reusable or single-use?

  The device data does not specify whether the MRT-150 QD Knee Coil is reusable or single-use, so this information would need to be obtained directly from the manufacturer.