FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

VISIUS WIRELESS COILS, 1.5T/ VISIUS WIRELESS COILS, 3T

K Number: K123091 · Decision Dec 27, 2012
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
14
Review Days
86

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Basic Information

Device Name
VISIUS WIRELESS COILS, 1.5T/ VISIUS WIRELESS COILS, 3T
K Number
K123091
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imris, Inc.
Date Received
October 2, 2012
Decision Date
December 27, 2012
Product Code
MOS
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
MOS Coil, Magnetic Resonance, Specialty

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K121997 IMRIS ONCOLOGY PACKAGE
K113748 IMRIS MR/X-RAY HEAD FIXATION DEVICE (HFD)
K103493 HEAD FIATION DEVICE (HFD 100)
K103506 1.5T HEAD COIL (HC150), 3T HEAD COIL (HC300)
K101813 IMRX SYSTEM V1 AND IMRISNV/IMRISCARDIO
K091166 IMRX
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