FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

IMATRON C-100 ULTRAFAST CT SCANNER

K Number: K872615 · Decision Sep 23, 1987
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
11
Review Days
79

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Basic Information

Device Name
IMATRON C-100 ULTRAFAST CT SCANNER
K Number
K872615
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Imatron, Inc.
Date Received
July 6, 1987
Decision Date
September 23, 1987
Product Code
JAK
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JAK System, X-Ray, Tomography, Computed

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JAK), ordered by most recent decision date.

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Other Clearances by Imatron, Inc.

K Number Device Name
K001550 EBT ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNER SYSTEMS; ELECTRON BEAM SCANNER SYSTEM; ELECTR
K000359 EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150. C-150LXP OR C-150XP SCANNER SYSTEMS; ELECTRO
K992740 EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150, C-150LXP OR C-150XP SCANNER SYSTEMS
K972903 IMATRON ULTRA ACCESS WORKSTATION WITH CARDIAC SOFTWARE EXTENSIONS
K972879 ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION
K913352 C-150 ULTRAFAST CT SCANNER
K874934 UNIVERSAL EXAMINATION TABLE
K864046 C-IOO MOBILE CINE CT UNIT
K840131 COMPUTED TOMOGRAPHY CALIBRATION PHANT
K828669 COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100
Search all 11 clearances from Imatron, Inc. →