INVU by Nuvo
K-Number: K210025 · 2021-05-28
ApplicantNuvo- Group , Ltd.
Decision Date2021-05-28
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 2021-05-28 under approval 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. It is manufactured by Nuvo- Group , Ltd.. The 510(k) number is K210025.
When was INVU by Nuvo approved by the FDA?
INVU by Nuvo received FDA 510(k) clearance on 2021-05-28, under approval number K210025.
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.