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FDA 510(k)

Electronic Sphygmomanometer (Model: LT-P30)

K-Number: K220220 · 2022-10-03

ApplicantZhuhai Linte Medical Instrument Co., Ltd.
Decision Date2022-10-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Electronic Sphygmomanometer (Model: LT-P30) is a medical device manufactured by Zhuhai Linte Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2022-10-03 under approval number K220220. 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 Sphygmomanometer (Model: LT-P30)?

Electronic Sphygmomanometer (Model: LT-P30) is a medical device that received FDA 510(k) clearance on 2022-10-03. It is manufactured by Zhuhai Linte Medical Instrument Co., Ltd.. The 510(k) number is K220220.

When was Electronic Sphygmomanometer (Model: LT-P30) approved by the FDA?

Electronic Sphygmomanometer (Model: LT-P30) received FDA 510(k) clearance on 2022-10-03, under approval number K220220.

What company makes Electronic Sphygmomanometer (Model: LT-P30)?

Electronic Sphygmomanometer (Model: LT-P30) is manufactured by Zhuhai Linte Medical Instrument Co., Ltd..

What is the FDA product code for Electronic Sphygmomanometer (Model: LT-P30)?

The FDA product code for Electronic Sphygmomanometer (Model: LT-P30) 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.

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