LiverMultiScan 2.1
by Perspectum
LiverMultiScan 2.1 is a Class II device made by Perspectum, cleared under FDA 510(k) K172685 on 21 Nov 2017 and listed in FDA GUDID since 4 Jul 2018 (UDI-DI B554LMS2100), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB554LMS2100 | Date4 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172685 | Date21 Nov 2017 | StatusActive |
Official records
- FDA 510(k) database K172685
Across registries
- FDA 510(k) K172685 decided 21 Nov 2017 Active
- FDA GUDID UDI-DI B554LMS2100 listed 4 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K172685
- Listed FDA GUDID B554LMS2100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LiverMultiScan
- Generic name
- Radiology DICOM image processing application software
- Model / reference
- 2.1
- Primary DI / UDI-DI
- B554LMS2100
- 510(k) Number
- FDA product code
- LNH
- GMDN term
- Radiology DICOM image processing application software
- Device class
- Class II
- Regulation number
- 892.1000
- GUDID distribution status
- In Commercial Distribution
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