2430MCA with Xmaru W
K-Number: K202902 · 2021-06-21
ApplicantRayence Co., Ltd.
Decision Date2021-06-21
Product CodeMUE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
2430MCA with Xmaru W is a medical device manufactured by Rayence Co., Ltd.. It received FDA 510(k) clearance on 2021-06-21 under approval number K202902. The device is classified under product code MUE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 2430MCA with Xmaru W?
2430MCA with Xmaru W is a medical device that received FDA 510(k) clearance on 2021-06-21. It is manufactured by Rayence Co., Ltd.. The 510(k) number is K202902.
When was 2430MCA with Xmaru W approved by the FDA?
2430MCA with Xmaru W received FDA 510(k) clearance on 2021-06-21, under approval number K202902.
What company makes 2430MCA with Xmaru W?
2430MCA with Xmaru W is manufactured by Rayence Co., Ltd..
What is the FDA product code for 2430MCA with Xmaru W?
The FDA product code for 2430MCA with Xmaru W is MUE.
Other Devices by Rayence Co., Ltd.
Related Devices (Code: MUE)
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.