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FDA 510(k)

Electronic Blood Pressure Monitor

K-Number: K182495 · 2019-03-03

Decision Date2019-03-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Electronic Blood Pressure Monitor is a medical device manufactured by Shenzhen Jumper Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2019-03-03 under approval number K182495. 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 Electronic Blood Pressure Monitor?

Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-03-03. It is manufactured by Shenzhen Jumper Medical Equipment Co., Ltd.. The 510(k) number is K182495.

When was Electronic Blood Pressure Monitor approved by the FDA?

Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2019-03-03, under approval number K182495.

What company makes Electronic Blood Pressure Monitor?

Electronic Blood Pressure Monitor is manufactured by Shenzhen Jumper Medical Equipment Co., Ltd..

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

The FDA product code for Electronic Blood Pressure Monitor is DXN.

Related Clinical Trials

Related PubMed Literature

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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.