FDA 510(k)

Maxxi Snore Sensor

K-Number: K191095 · 2020-01-16

Decision Date2020-01-16

Product CodeMNR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

Maxxi Snore Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Neurovirtual USA, Inc.. It received FDA 510(k) clearance on 2020-01-16 under 510(k) 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. The listed applicant is Neurovirtual USA, Inc.. The 510(k) number is K191095.

When did Maxxi Snore Sensor receive FDA 510(k) clearance?

Maxxi Snore Sensor received FDA 510(k) clearance on 2020-01-16, under 510(k) number K191095.

Who is the listed applicant for Maxxi Snore Sensor?

The FDA 510(k) record lists Neurovirtual USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Maxxi Snore Sensor?

The FDA product code for Maxxi Snore Sensor is MNR.

Other records listing Neurovirtual USA, Inc. 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.

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Official Source

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