FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

HepaFat-AI

K Number: K201039 · Decision Dec 7, 2020
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
7
Review Days
231

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HepaFat-AI
K Number
K201039
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
April 20, 2020
Decision Date
December 7, 2020
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

Other 510(k) clearances with the same product code (LNH), ordered by most recent decision date.

View all

Other Clearances by Resonance Health Analysis Services Pty, Ltd.

K Number Device Name
K231459 HepaFatSmart (V2.0.0)
K213776 LiverSmart
K182218 FerriSmart Analysis System
K122035 HEPAFAT SCAN
DEN130012 FERRISCAN R2-MRI ANALYSIS SYSTEM
K111222 MRI-Q SYSTEM