Relivion
K-Number: K203419 · 2021-02-16
ApplicantNeurolief , Ltd.
Decision Date2021-02-16
Product CodePCC
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Relivion is a medical device manufactured by Neurolief , Ltd.. It received FDA 510(k) clearance on 2021-02-16 under approval number K203419. The device is classified under product code PCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Relivion?
Relivion is a medical device that received FDA 510(k) clearance on 2021-02-16. It is manufactured by Neurolief , Ltd.. The 510(k) number is K203419.
When was Relivion approved by the FDA?
Relivion received FDA 510(k) clearance on 2021-02-16, under approval number K203419.
What company makes Relivion?
Relivion is manufactured by Neurolief , Ltd..
What is the FDA product code for Relivion?
The FDA product code for Relivion is PCC.
Other Devices by Neurolief , Ltd.
Related Devices (Code: PCC)
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.