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

SENSE HEAD 16 MODEL 800647, SENSE SPINE 16 MODEL 800646; SENSE TORSO 16 MODEL 800645

K Number: K122897 · Decision Dec 21, 2012
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
29
Review Days
91

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Basic Information

Device Name
SENSE HEAD 16 MODEL 800647, SENSE SPINE 16 MODEL 800646; SENSE TORSO 16 MODEL 800645
K Number
K122897
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Invivo Corporation
Date Received
September 21, 2012
Decision Date
December 21, 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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