FDA 510(k)

INVU by Nuvo

K-Number: K210025 · 2021-05-28

Decision Date2021-05-28

Product CodeLQK

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

INVU by Nuvo is the device name listed in this FDA 510(k) record. The listed applicant is Nuvo- Group , Ltd.. It received FDA 510(k) clearance on 2021-05-28 under 510(k) number K210025. The device is classified under product code LQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVU by Nuvo?

INVU by Nuvo is a medical device that received FDA 510(k) clearance on 2021-05-28. The listed applicant is Nuvo- Group , Ltd.. The 510(k) number is K210025.

When did INVU by Nuvo receive FDA 510(k) clearance?

INVU by Nuvo received FDA 510(k) clearance on 2021-05-28, under 510(k) number K210025.

Who is the listed applicant for INVU by Nuvo?

The FDA 510(k) record lists Nuvo- Group , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVU by Nuvo?

The FDA product code for INVU by Nuvo is LQK.

Other records listing Nuvo- Group , Ltd. 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.

K221046Invu by Nuvo K191401PregSense

Related Devices (Code: LQK)

K221046Invu by NuvoNuvo- Group , Ltd.K191401PregSenseNuvo- Group , Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.