Reusable Blood Pressure Cuff
K-Number: K233276 · 2023-12-21
Decision Date2023-12-21
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Reusable Blood Pressure Cuff is a medical device manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2023-12-21 under approval number K233276. 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 Reusable Blood Pressure Cuff?
Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2023-12-21. It is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K233276.
When was Reusable Blood Pressure Cuff approved by the FDA?
Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2023-12-21, under approval number K233276.
What company makes Reusable Blood Pressure Cuff?
Reusable Blood Pressure Cuff is manufactured by Suzhou Minhua Medical Apparatus Supplies Co., Ltd..
What is the FDA product code for Reusable Blood Pressure Cuff?
The FDA product code for Reusable Blood Pressure Cuff 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.