Home / 510(k) Clearances / K828669

510(k) K828669

COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100 by Imatron, Inc.

K828669 is an FDA 510(k) premarket notification submitted by Imatron, Inc. for the device "COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100". The FDA issued a decision of Substantially Equivalent on January 14, 1983. Imatron, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 14, 1983
Date Received
November 30, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Imatron, Inc.

  • K001550 — EBT ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNER SYSTE (December 11, 2000)
  • K000359 — EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150. C-15 (March 17, 2000)
  • K992740 — EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-15 (November 9, 1999)
  • K972903 — IMATRON ULTRA ACCESS WORKSTATION WITH CARDIAC SOFTWARE EXTENSIONS (November 4, 1997)
  • K972879 — ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION (October 15, 1997)
  • K913352 — C-150 ULTRAFAST CT SCANNER (November 29, 1991)
  • K874934 — UNIVERSAL EXAMINATION TABLE (January 19, 1988)
  • K872615 — IMATRON C-100 ULTRAFAST CT SCANNER (September 23, 1987)
  • K864046 — C-IOO MOBILE CINE CT UNIT (November 10, 1986)
  • K840131 — COMPUTED TOMOGRAPHY CALIBRATION PHANT (February 21, 1984)

FDA data resources