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

IB NEURO, VERSION 1.0

K Number: K080762 · Decision May 15, 2008
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
4
Review Days
58

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Basic Information

Device Name
IB NEURO, VERSION 1.0
K Number
K080762
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imaging Biometrics, LLC
Date Received
March 18, 2008
Decision Date
May 15, 2008
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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K201092 LSN
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