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FDA 510(k)

LiverMultiScan (v6.0)

K-Number: K253413 · 2026-03-09

ApplicantPerspectum, Ltd.
Decision Date2026-03-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LiverMultiScan (v6.0) is a medical device manufactured by Perspectum, Ltd.. It received FDA 510(k) clearance on 2026-03-09 under approval number K253413. 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 (v6.0)?

LiverMultiScan (v6.0) is a medical device that received FDA 510(k) clearance on 2026-03-09. It is manufactured by Perspectum, Ltd.. The 510(k) number is K253413.

When was LiverMultiScan (v6.0) approved by the FDA?

LiverMultiScan (v6.0) received FDA 510(k) clearance on 2026-03-09, under approval number K253413.

What company makes LiverMultiScan (v6.0)?

LiverMultiScan (v6.0) is manufactured by Perspectum, Ltd..

What is the FDA product code for LiverMultiScan (v6.0)?

The FDA product code for LiverMultiScan (v6.0) is LNH.

Other Devices by Perspectum, Ltd.

K202170LiverMultiScan K203280Hepatica v1 (Hepatica v1.0.0) K212565CoverScan v1 K241925VitruvianScan (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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