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 | Device Class | Medical Specialty |
|---|---|---|---|
| LNH | System, Nuclear Magnetic Resonance Imaging | FDA class 2 | Radiology |
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Other Clearances by Resonance Health Analysis Services Pty, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K231459 | HepaFatSmart (V2.0.0) | Jun 20, 2023 | Substantially Equivalent |
| K213776 | LiverSmart | Dec 29, 2021 | Substantially Equivalent |
| K201039 | HepaFat-AI | Dec 7, 2020 | Substantially Equivalent |
| K182218 | FerriSmart Analysis System | Nov 30, 2018 | Substantially Equivalent |
| DEN130012 | FERRISCAN R2-MRI ANALYSIS SYSTEM | Jan 23, 2013 | Unknown |
| K111222 | MRI-Q SYSTEM | Jul 28, 2011 | Substantially Equivalent |