FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
LiverMultiScan (LMSv3)
K Number: K190017
·
Decision Jun 27, 2019
Classifications
1
FEI Numbers
152
Registration Numbers
152
Same Product Code
1071
Applicant Total
3
Review Days
175
Basic Information
- Device Name
- LiverMultiScan (LMSv3)
- K Number
- K190017
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1000
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Perspectum Diagnostics Ltd
- Date Received
- January 3, 2019
- Decision Date
- June 27, 2019
- 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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