Aneroid Sphygmomanometer
K-Number: K230859 · 2023-06-28
Decision Date2023-06-28
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Aneroid Sphygmomanometer is a medical device manufactured by Wenzhou Kangshun Medical Devices Co.,Ltd. It received FDA 510(k) clearance on 2023-06-28 under approval number K230859. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2023-06-28. It is manufactured by Wenzhou Kangshun Medical Devices Co.,Ltd. The 510(k) number is K230859.
When was Aneroid Sphygmomanometer approved by the FDA?
Aneroid Sphygmomanometer received FDA 510(k) clearance on 2023-06-28, under approval number K230859.
What company makes Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer is manufactured by Wenzhou Kangshun Medical Devices Co.,Ltd.
What is the FDA product code for Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer is DXQ.
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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.