Imatron, Inc.

FDA Regulatory Profile

Imatron, Inc. appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 11, 2000.

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001550EBT ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNER SYSTEMS; ELECTRON BEAM SCDecember 11, 2000
K000359EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150. C-150LXP OR C-150XP SCANMarch 17, 2000
K992740EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNovember 9, 1999
K972903IMATRON ULTRA ACCESS WORKSTATION WITH CARDIAC SOFTWARE EXTENSIONSNovember 4, 1997
K972879ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTIONOctober 15, 1997
K913352C-150 ULTRAFAST CT SCANNERNovember 29, 1991
K874934UNIVERSAL EXAMINATION TABLEJanuary 19, 1988
K872615IMATRON C-100 ULTRAFAST CT SCANNERSeptember 23, 1987
K864046C-IOO MOBILE CINE CT UNITNovember 10, 1986
K840131COMPUTED TOMOGRAPHY CALIBRATION PHANTFebruary 21, 1984
K828669COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100January 14, 1983