Rayvolve
K-Number: K240845 · 2024-07-17
ApplicantAzmed Sas
Decision Date2024-07-17
Product CodeQBS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Rayvolve is a medical device manufactured by Azmed Sas. It received FDA 510(k) clearance on 2024-07-17 under approval number K240845. The device is classified under product code QBS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Rayvolve?
Rayvolve is a medical device that received FDA 510(k) clearance on 2024-07-17. It is manufactured by Azmed Sas. The 510(k) number is K240845.
When was Rayvolve approved by the FDA?
Rayvolve received FDA 510(k) clearance on 2024-07-17, under approval number K240845.
What company makes Rayvolve?
Rayvolve is manufactured by Azmed Sas.
What is the FDA product code for Rayvolve?
The FDA product code for Rayvolve is QBS.
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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.