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FDA 510(k)

LIVIA

K-Number: K183110 · 2020-05-04

ApplicantLifecare , Ltd.
Decision Date2020-05-04
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LIVIA is a medical device manufactured by Lifecare , Ltd.. It received FDA 510(k) clearance on 2020-05-04 under approval number K183110. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIVIA?

LIVIA is a medical device that received FDA 510(k) clearance on 2020-05-04. It is manufactured by Lifecare , Ltd.. The 510(k) number is K183110.

When was LIVIA approved by the FDA?

LIVIA received FDA 510(k) clearance on 2020-05-04, under approval number K183110.

What company makes LIVIA?

LIVIA is manufactured by Lifecare , Ltd..

What is the FDA product code for LIVIA?

The FDA product code for LIVIA is NUH.

Other Devices by Lifecare , Ltd.

K163153Livia

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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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