Medical Device Manufacturer · US , South San Fransisco , CA

Imatron, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1983

Total

Cleared

Denied

Imatron, Inc. has 11 FDA 510(k) cleared radiology devices. Based in South San Fransisco, US.

Historical record: 11 cleared submissions from 1983 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 - Imatron, Inc.

11 devices

1-11 of 11

Cleared Dec 11, 2000

EBT ULTRAFAST CT SCANNER SYSTEM

K001550 · LLZ

Radiology · 207d

Cleared Mar 17, 2000

EBT ULTRAFAST CT SCANNER SYSTEM

K000359 · JAK

Radiology · 42d

Cleared Nov 09, 1999

EBT ULTRAFAST CT SCANNER SYSTEM

K992740 · JAK

Radiology · 85d

Cleared Nov 04, 1997

IMATRON ULTRA ACCESS WORKSTATION WITH CARDIAC SOFTWARE EXTENSIONS

C-150 ULTRAFAST CT SCANNER

K913352 · JAK

Radiology · 126d

Cleared Jan 19, 1988

UNIVERSAL EXAMINATION TABLE

K874934 · KXJ

Radiology · 46d

Cleared Sep 23, 1987

IMATRON C-100 ULTRAFAST CT SCANNER

K872615 · JAK

Radiology · 79d

Cleared Nov 10, 1986

C-IOO MOBILE CINE CT UNIT

K864046 · JAK

Radiology · 25d

Cleared Feb 21, 1984

COMPUTED TOMOGRAPHY CALIBRATION PHANT

K840131 · IXG

Radiology · 42d

Cleared Jan 14, 1983

COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100

K828669

Radiology · 45d

Imatron, Inc. - FDA 510(k) Cleared Devices

Filters