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FDA 510(k)

Digital Automatic Blood Pressure Monitor MD3600

K-Number: K163679 · 2017-06-07

Decision Date2017-06-07
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Digital Automatic Blood Pressure Monitor MD3600 is a medical device manufactured by Grandway Technology (Shenzhen) Limited. It received FDA 510(k) clearance on 2017-06-07 under approval number K163679. 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 Digital Automatic Blood Pressure Monitor MD3600?

Digital Automatic Blood Pressure Monitor MD3600 is a medical device that received FDA 510(k) clearance on 2017-06-07. It is manufactured by Grandway Technology (Shenzhen) Limited. The 510(k) number is K163679.

When was Digital Automatic Blood Pressure Monitor MD3600 approved by the FDA?

Digital Automatic Blood Pressure Monitor MD3600 received FDA 510(k) clearance on 2017-06-07, under approval number K163679.

What company makes Digital Automatic Blood Pressure Monitor MD3600?

Digital Automatic Blood Pressure Monitor MD3600 is manufactured by Grandway Technology (Shenzhen) Limited.

What is the FDA product code for Digital Automatic Blood Pressure Monitor MD3600?

The FDA product code for Digital Automatic Blood Pressure Monitor MD3600 is DXN.

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Official Source

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