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FDA 510(k)

Evie Med Ring

K-Number: K241090 · 2024-11-29

Decision Date2024-11-29
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Evie Med Ring is the device name listed in this FDA 510(k) record. The listed applicant is Movano Inc. Dba Movano Health. It received FDA 510(k) clearance on 2024-11-29 under 510(k) 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. The listed applicant is Movano Inc. Dba Movano Health. The 510(k) number is K241090.

When did Evie Med Ring receive FDA 510(k) clearance?

Evie Med Ring received FDA 510(k) clearance on 2024-11-29, under 510(k) number K241090.

Who is the listed applicant for Evie Med Ring?

The FDA 510(k) record lists Movano Inc. Dba Movano Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Evie Med Ring?

The FDA product code for Evie Med Ring is DQA.

Related Devices (Code: DQA)

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.

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.