Maxxi Snore Sensor
K-Number: K191095 · 2020-01-16
ApplicantNeurovirtual USA, Inc.
Decision Date2020-01-16
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Maxxi Snore Sensor is a medical device manufactured by Neurovirtual USA, Inc.. It received FDA 510(k) clearance on 2020-01-16 under approval number K191095. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Maxxi Snore Sensor?
Maxxi Snore Sensor is a medical device that received FDA 510(k) clearance on 2020-01-16. It is manufactured by Neurovirtual USA, Inc.. The 510(k) number is K191095.
When was Maxxi Snore Sensor approved by the FDA?
Maxxi Snore Sensor received FDA 510(k) clearance on 2020-01-16, under approval number K191095.
What company makes Maxxi Snore Sensor?
Maxxi Snore Sensor is manufactured by Neurovirtual USA, Inc..
What is the FDA product code for Maxxi Snore Sensor?
The FDA product code for Maxxi Snore Sensor is MNR.
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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.