The Wrist-Type Fully Automatic Digital Blood Pressure Monitors
K-Number: K170666 · 2017-11-22
ApplicantJoytech Healthcare Co. , Ltd.
Decision Date2017-11-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
The Wrist-Type Fully Automatic Digital Blood Pressure Monitors is a medical device manufactured by Joytech Healthcare Co. , Ltd.. It received FDA 510(k) clearance on 2017-11-22 under approval number K170666. 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 The Wrist-Type Fully Automatic Digital Blood Pressure Monitors?
The Wrist-Type Fully Automatic Digital Blood Pressure Monitors is a medical device that received FDA 510(k) clearance on 2017-11-22. It is manufactured by Joytech Healthcare Co. , Ltd.. The 510(k) number is K170666.
When was The Wrist-Type Fully Automatic Digital Blood Pressure Monitors approved by the FDA?
The Wrist-Type Fully Automatic Digital Blood Pressure Monitors received FDA 510(k) clearance on 2017-11-22, under approval number K170666.
What company makes The Wrist-Type Fully Automatic Digital Blood Pressure Monitors?
The Wrist-Type Fully Automatic Digital Blood Pressure Monitors is manufactured by Joytech Healthcare Co. , Ltd..
What is the FDA product code for The Wrist-Type Fully Automatic Digital Blood Pressure Monitors?
The FDA product code for The Wrist-Type Fully Automatic Digital Blood Pressure Monitors 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.