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FDA 510(k)

LiverMultiScan

K-Number: K172685 · 2017-11-21

ApplicantPerspectum Diagnostics, Ltd.
Decision Date2017-11-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LiverMultiScan is a medical device manufactured by Perspectum Diagnostics, Ltd.. It received FDA 510(k) clearance on 2017-11-21 under approval number K172685. 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?

LiverMultiScan is a medical device that received FDA 510(k) clearance on 2017-11-21. It is manufactured by Perspectum Diagnostics, Ltd.. The 510(k) number is K172685.

When was LiverMultiScan approved by the FDA?

LiverMultiScan received FDA 510(k) clearance on 2017-11-21, under approval number K172685.

What company makes LiverMultiScan?

LiverMultiScan is manufactured by Perspectum Diagnostics, Ltd..

What is the FDA product code for LiverMultiScan?

The FDA product code for LiverMultiScan is LNH.

Other Devices by Perspectum Diagnostics, Ltd.

K190017LiverMultiScan (LMSv3) 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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