FDA 510(k)

Maxxi Rip Sensor

K-Number: K171304 · 2019-06-24

Decision Date2019-06-24

Product CodeMNR

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

Maxxi Rip 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 2019-06-24 under 510(k) 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. The listed applicant is Neurovirtual USA, Inc.. The 510(k) number is K171304.

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

Maxxi Rip Sensor received FDA 510(k) clearance on 2019-06-24, under 510(k) number K171304.

Who is the listed applicant for Maxxi Rip 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 Rip Sensor?

The FDA product code for Maxxi Rip 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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