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FDA 510(k)

LiverMultiScan (LMSv3)

K-Number: K190017 · 2019-06-27

ApplicantPerspectum Diagnostics, Ltd.
Decision Date2019-06-27
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LiverMultiScan (LMSv3) is a medical device manufactured by Perspectum Diagnostics, Ltd.. It received FDA 510(k) clearance on 2019-06-27 under approval number K190017. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LiverMultiScan (LMSv3)?

LiverMultiScan (LMSv3) is a medical device that received FDA 510(k) clearance on 2019-06-27. It is manufactured by Perspectum Diagnostics, Ltd.. The 510(k) number is K190017.

When was LiverMultiScan (LMSv3) approved by the FDA?

LiverMultiScan (LMSv3) received FDA 510(k) clearance on 2019-06-27, under approval number K190017.

What company makes LiverMultiScan (LMSv3)?

LiverMultiScan (LMSv3) is manufactured by Perspectum Diagnostics, Ltd..

What is the FDA product code for LiverMultiScan (LMSv3)?

The FDA product code for LiverMultiScan (LMSv3) is LNH.

Other Devices by Perspectum Diagnostics, Ltd.

K172685LiverMultiScan K183133MRCP+ v1.0

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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