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FDA 510(k)

Livia

K-Number: K163153 · 2017-06-28

ApplicantLifecare , Ltd.
Decision Date2017-06-28
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Livia is a medical device manufactured by Lifecare , Ltd.. It received FDA 510(k) clearance on 2017-06-28 under approval number K163153. 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 2017-06-28. It is manufactured by Lifecare , Ltd.. The 510(k) number is K163153.

When was Livia approved by the FDA?

Livia received FDA 510(k) clearance on 2017-06-28, under approval number K163153.

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.

K183110LIVIA

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Official Source

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

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