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FDA 510(k)

Wrist Type Automatic Blood Pressure Monitor

K-Number: K172972 · 2018-03-02

Decision Date2018-03-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Wrist Type Automatic Blood Pressure Monitor is a medical device manufactured by Shenzhen Jiacom Technology CO ., Ltd.. It received FDA 510(k) clearance on 2018-03-02 under approval number K172972. 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 Wrist Type Automatic Blood Pressure Monitor?

Wrist Type Automatic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2018-03-02. It is manufactured by Shenzhen Jiacom Technology CO ., Ltd.. The 510(k) number is K172972.

When was Wrist Type Automatic Blood Pressure Monitor approved by the FDA?

Wrist Type Automatic Blood Pressure Monitor received FDA 510(k) clearance on 2018-03-02, under approval number K172972.

What company makes Wrist Type Automatic Blood Pressure Monitor?

Wrist Type Automatic Blood Pressure Monitor is manufactured by Shenzhen Jiacom Technology CO ., Ltd..

What is the FDA product code for Wrist Type Automatic Blood Pressure Monitor?

The FDA product code for Wrist Type Automatic Blood Pressure Monitor is DXN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.