Electronic Sphygmomanometers
K-Number: K222394 · 2023-03-03
Decision Date2023-03-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Electronic Sphygmomanometers is a medical device manufactured by Qingdao Yasee Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2023-03-03 under approval number K222394. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Electronic Sphygmomanometers?
Electronic Sphygmomanometers is a medical device that received FDA 510(k) clearance on 2023-03-03. It is manufactured by Qingdao Yasee Medical Device Co., Ltd.. The 510(k) number is K222394.
When was Electronic Sphygmomanometers approved by the FDA?
Electronic Sphygmomanometers received FDA 510(k) clearance on 2023-03-03, under approval number K222394.
What company makes Electronic Sphygmomanometers?
Electronic Sphygmomanometers is manufactured by Qingdao Yasee Medical Device Co., Ltd..
What is the FDA product code for Electronic Sphygmomanometers?
The FDA product code for Electronic Sphygmomanometers is DXN.
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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.