Evie Med Ring
K-Number: K241090 · 2024-11-29
ApplicantMovano Inc. Dba Movano Health
Decision Date2024-11-29
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Evie Med Ring is a medical device manufactured by Movano Inc. Dba Movano Health. It received FDA 510(k) clearance on 2024-11-29 under approval number K241090. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Evie Med Ring?
Evie Med Ring is a medical device that received FDA 510(k) clearance on 2024-11-29. It is manufactured by Movano Inc. Dba Movano Health. The 510(k) number is K241090.
When was Evie Med Ring approved by the FDA?
Evie Med Ring received FDA 510(k) clearance on 2024-11-29, under approval number K241090.
What company makes Evie Med Ring?
Evie Med Ring is manufactured by Movano Inc. Dba Movano Health.
What is the FDA product code for Evie Med Ring?
The FDA product code for Evie Med Ring is DQA.
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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.