A&D Medical Blood Pressure Monitors
K-Number: K173191 · 2019-03-21
ApplicantA&D Company, Ltd.
Decision Date2019-03-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
A&D Medical Blood Pressure Monitors is a medical device manufactured by A&D Company, Ltd.. It received FDA 510(k) clearance on 2019-03-21 under approval number K173191. 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 A&D Medical Blood Pressure Monitors?
A&D Medical Blood Pressure Monitors is a medical device that received FDA 510(k) clearance on 2019-03-21. It is manufactured by A&D Company, Ltd.. The 510(k) number is K173191.
When was A&D Medical Blood Pressure Monitors approved by the FDA?
A&D Medical Blood Pressure Monitors received FDA 510(k) clearance on 2019-03-21, under approval number K173191.
What company makes A&D Medical Blood Pressure Monitors?
A&D Medical Blood Pressure Monitors is manufactured by A&D Company, Ltd..
What is the FDA product code for A&D Medical Blood Pressure Monitors?
The FDA product code for A&D Medical 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.