FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

SIGNA Pioneer

K Number: K143345 · Decision Jul 10, 2015
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
10
Review Days
231

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Basic Information

Device Name
SIGNA Pioneer
K Number
K143345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Healthcare Japan Corporation
Date Received
November 21, 2014
Decision Date
July 10, 2015
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

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