Imatron, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imatron, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
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
Cleared
Dec 11, 2000
EBT ULTRAFAST CT SCANNER SYSTEM
Radiology
207d
Cleared
Mar 17, 2000
EBT ULTRAFAST CT SCANNER SYSTEM
Radiology
42d
Cleared
Nov 09, 1999
EBT ULTRAFAST CT SCANNER SYSTEM
Radiology
85d
Cleared
Nov 04, 1997
IMATRON ULTRA ACCESS WORKSTATION WITH CARDIAC SOFTWARE EXTENSIONS
Radiology
90d
Cleared
Oct 15, 1997
ULTRAFAST CT SCANNER
Radiology
71d
Cleared
Nov 29, 1991
C-150 ULTRAFAST CT SCANNER
Radiology
126d
Cleared
Jan 19, 1988
UNIVERSAL EXAMINATION TABLE
Radiology
46d
Cleared
Sep 23, 1987
IMATRON C-100 ULTRAFAST CT SCANNER
Radiology
79d
Cleared
Nov 10, 1986
C-IOO MOBILE CINE CT UNIT
Radiology
25d
Cleared
Feb 21, 1984
COMPUTED TOMOGRAPHY CALIBRATION PHANT
Radiology
42d
Cleared
Jan 14, 1983
COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100
Radiology
45d