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FDA 510(k)

Arm Blood Pressure Monitor

K-Number: K193456 · 2020-07-16

Decision Date2020-07-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Arm Blood Pressure Monitor is a medical device manufactured by Ningbo Ranor Medical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-07-16 under approval number K193456. 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 Blood Pressure Monitor?

Arm Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-07-16. It is manufactured by Ningbo Ranor Medical Science & Technology Co., Ltd.. The 510(k) number is K193456.

When was Arm Blood Pressure Monitor approved by the FDA?

Arm Blood Pressure Monitor received FDA 510(k) clearance on 2020-07-16, under approval number K193456.

What company makes Arm Blood Pressure Monitor?

Arm Blood Pressure Monitor is manufactured by Ningbo Ranor Medical Science & Technology Co., Ltd..

What is the FDA product code for Arm Blood Pressure Monitor?

The FDA product code for Arm 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.