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FDA 510(k)

Arm automatic blood pressure monitor

K-Number: K161712 · 2017-04-05

Decision Date2017-04-05
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Arm automatic blood pressure monitor is a medical device manufactured by Shenzhen Pump Medical System Co., Ltd.. It received FDA 510(k) clearance on 2017-04-05 under approval number K161712. 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 Arm automatic blood pressure monitor?

Arm automatic blood pressure monitor is a medical device that received FDA 510(k) clearance on 2017-04-05. It is manufactured by Shenzhen Pump Medical System Co., Ltd.. The 510(k) number is K161712.

When was Arm automatic blood pressure monitor approved by the FDA?

Arm automatic blood pressure monitor received FDA 510(k) clearance on 2017-04-05, under approval number K161712.

What company makes Arm automatic blood pressure monitor?

Arm automatic blood pressure monitor is manufactured by Shenzhen Pump Medical System Co., Ltd..

What is the FDA product code for Arm automatic blood pressure monitor?

The FDA product code for Arm 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.