LIVIA
K-Number: K183110 · 2020-05-04
Device Summary
Frequently Asked Questions
What is the LIVIA?
LIVIA is a medical device that received FDA 510(k) clearance on 2020-05-04. The listed applicant is Lifecare , Ltd.. The 510(k) number is K183110.
When did LIVIA receive FDA 510(k) clearance?
LIVIA received FDA 510(k) clearance on 2020-05-04, under 510(k) number K183110.
Who is the listed applicant for LIVIA?
The FDA 510(k) record lists Lifecare , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIVIA?
The FDA product code for LIVIA is NUH.
Other records listing Lifecare , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NUH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.