Belun Ring
K-Number: K191417 · 2019-10-10
ApplicantBelun Technology Company Limited
Decision Date2019-10-10
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Belun Ring is a medical device manufactured by Belun Technology Company Limited. It received FDA 510(k) clearance on 2019-10-10 under approval number K191417. 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 Belun Ring?
Belun Ring is a medical device that received FDA 510(k) clearance on 2019-10-10. It is manufactured by Belun Technology Company Limited. The 510(k) number is K191417.
When was Belun Ring approved by the FDA?
Belun Ring received FDA 510(k) clearance on 2019-10-10, under approval number K191417.
What company makes Belun Ring?
Belun Ring is manufactured by Belun Technology Company Limited.
What is the FDA product code for Belun Ring?
The FDA product code for Belun Ring is DQA.
Related Clinical Trials
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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.