LiverMultiScan
K-Number: K202170 · 2020-10-02
ApplicantPerspectum, Ltd.
Decision Date2020-10-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
LiverMultiScan is a medical device manufactured by Perspectum, Ltd.. It received FDA 510(k) clearance on 2020-10-02 under approval number K202170. 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 2020-10-02. It is manufactured by Perspectum, Ltd.. The 510(k) number is K202170.
When was LiverMultiScan approved by the FDA?
LiverMultiScan received FDA 510(k) clearance on 2020-10-02, under approval number K202170.
What company makes LiverMultiScan?
LiverMultiScan is manufactured by Perspectum, Ltd..
What is the FDA product code for LiverMultiScan?
The FDA product code for LiverMultiScan is LNH.
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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.