FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

COMPUTED TOMOGRAPHY CALIBRATION PHANT

K Number: K840131 · Decision Feb 21, 1984
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
3
Applicant Total
11
Review Days
42

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Basic Information

Device Name
COMPUTED TOMOGRAPHY CALIBRATION PHANT
K Number
K840131
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1950
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Imatron, Inc.
Date Received
January 10, 1984
Decision Date
February 21, 1984
Product Code
IXG
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
IXG Phantom, Anthropomorphic, Radiographic

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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
K872615 IMATRON C-100 ULTRAFAST CT SCANNER
K864046 C-IOO MOBILE CINE CT UNIT
K828669 COMPUTED CINETOMOGRAPHY SCANNER, MODEL C-100
Search all 11 clearances from Imatron, Inc. →