Maxxi Rip Sensor
K-Number: K171304 · 2019-06-24
ApplicantNeurovirtual USA, Inc.
Decision Date2019-06-24
Product CodeMNR
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Maxxi Rip Sensor is a medical device manufactured by Neurovirtual USA, Inc.. It received FDA 510(k) clearance on 2019-06-24 under approval number K171304. 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 Rip Sensor?
Maxxi Rip Sensor is a medical device that received FDA 510(k) clearance on 2019-06-24. It is manufactured by Neurovirtual USA, Inc.. The 510(k) number is K171304.
When was Maxxi Rip Sensor approved by the FDA?
Maxxi Rip Sensor received FDA 510(k) clearance on 2019-06-24, under approval number K171304.
What company makes Maxxi Rip Sensor?
Maxxi Rip Sensor is manufactured by Neurovirtual USA, Inc..
What is the FDA product code for Maxxi Rip Sensor?
The FDA product code for Maxxi Rip 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.