Perspectum Diagnostics, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 2
What Perspectum Diagnostics, Ltd. makes
Perspectum Diagnostics, Ltd. manufactures the LiverMultiScan and its updated version, LiverMultiScan (LMSv3), which are non-invasive imaging devices used for assessing liver fibrosis and steatosis in patients. These tools provide quantitative measurements to support clinical decision-making regarding liver disease progression.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is authorised for use in the United States, where the manufacturer is based.
Catalogue
LiverMultiScan Ref K172685
Regimes: 510(k) Registry: 510(k)LiverMultiScan (LMSv3) Ref K190017
Regimes: CE MDR CE MDD 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perspectum Diagnostics, Ltd. have in the registry?
The registry currently lists 2 devices for Perspectum Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perspectum Diagnostics, Ltd.'s devices?
Among its 2 most recently registered devices, Perspectum Diagnostics, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Perspectum Diagnostics, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Perspectum Diagnostics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Perspectum Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Perspectum Diagnostics, Ltd. include LiverMultiScan and LiverMultiScan (LMSv3).