Non-invasive blood pressure measurement systems
K-Number: K173024 · 2018-08-22
ApplicantJoytech Healthcare Co. , Ltd.
Decision Date2018-08-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Non-invasive blood pressure measurement systems is a medical device manufactured by Joytech Healthcare Co. , Ltd.. It received FDA 510(k) clearance on 2018-08-22 under approval number K173024. 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 Non-invasive blood pressure measurement systems?
Non-invasive blood pressure measurement systems is a medical device that received FDA 510(k) clearance on 2018-08-22. It is manufactured by Joytech Healthcare Co. , Ltd.. The 510(k) number is K173024.
When was Non-invasive blood pressure measurement systems approved by the FDA?
Non-invasive blood pressure measurement systems received FDA 510(k) clearance on 2018-08-22, under approval number K173024.
What company makes Non-invasive blood pressure measurement systems?
Non-invasive blood pressure measurement systems is manufactured by Joytech Healthcare Co. , Ltd..
What is the FDA product code for Non-invasive blood pressure measurement systems?
The FDA product code for Non-invasive blood pressure measurement systems 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.