Medical Device Manufacturer · US , South San Francisco , CA

Toshiba America Mri, Inc. - FDA 510(k) Cleared Devices

68 submissions · 68 cleared · Since 1990

Total

Cleared

Denied

Toshiba America Mri, Inc. has 68 FDA 510(k) cleared radiology devices. Based in South San Francisco, US.

Historical record: 68 cleared submissions from 1990 to 2000.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Toshiba America Mri, Inc.

68 devices

1-12 of 68

Cleared Oct 26, 2000

EXCELART WITH PIANISSIMO, MODEL MRT-1501/P3

EXCELART WITH PIANISSIMO

K993803 · LNH

Radiology · 89d

Cleared Jan 18, 2000

OPART/PRODIGA, OPART/PROTENZA, OPART/PARAGON

EXTRA LARGE BODY COIL FOR OPART (MRT-600)

FLEXART,FLEXART/HYPER, VISART, VISART/HYPER

K983110 · LNH

Radiology · 174d

Cleared Jul 14, 1998

OPART (MRT-600) VERSIONS 2 SOFTWARE UPGRADE

K981475 · LNH

Radiology · 81d

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Toshiba America Mri, Inc. - FDA 510(k) Cleared Devices

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