FDA 510(k)

Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U

Número K: K170454 · 2017-10-25

Data da decisão2017-10-25

Código do produtoDXN

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U is the device name listed in this FDA 510(k) record. The listed applicant is Honsun (Nantong) Co., Ltd.. It received FDA 510(k) clearance on 2017-10-25 under 510(k) number K170454. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U?

Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U is a medical device that received FDA 510(k) clearance on 2017-10-25. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K170454.

When did Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U receive FDA 510(k) clearance?

Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U received FDA 510(k) clearance on 2017-10-25, under 510(k) number K170454.

Who is the listed applicant for Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U?

The FDA 510(k) record lists Honsun (Nantong) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U?

The FDA product code for Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U is DXN.

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