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

HEPAFAT SCAN

K Number: K122035 · Decision Dec 13, 2013
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
7
Review Days
520

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Basic Information

Device Name
HEPAFAT SCAN
K Number
K122035
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Resonance Health Analysis Services Pty, Ltd.
Date Received
July 11, 2012
Decision Date
December 13, 2013
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

Similar 510(k) Clearances

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Other Clearances by Resonance Health Analysis Services Pty, Ltd.

K Number Device Name
K231459 HepaFatSmart (V2.0.0)
K213776 LiverSmart
K201039 HepaFat-AI
K182218 FerriSmart Analysis System
DEN130012 FERRISCAN R2-MRI ANALYSIS SYSTEM
K111222 MRI-Q SYSTEM