Invu by Nuvo
K-Number: K221046 · 2022-05-06
ApplicantNuvo- Group , Ltd.
Decision Date2022-05-06
Product CodeLQK
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Invu by Nuvo is a medical device manufactured by Nuvo- Group , Ltd.. It received FDA 510(k) clearance on 2022-05-06 under approval number K221046. 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 2022-05-06. It is manufactured by Nuvo- Group , Ltd.. The 510(k) number is K221046.
When was Invu by Nuvo approved by the FDA?
Invu by Nuvo received FDA 510(k) clearance on 2022-05-06, under approval number K221046.
What company makes Invu by Nuvo?
Invu by Nuvo is manufactured by Nuvo- Group , Ltd..
What is the FDA product code for Invu by Nuvo?
The FDA product code for Invu by Nuvo is LQK.
Other Devices by Nuvo- Group , Ltd.
Related Devices (Code: LQK)
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.