FDA 510(k)

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)

N.º K: K251795 · 2025-10-09

Fecha de decisión2025-10-09

Código de productoDXN

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) 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 2025-10-09 under 510(k) number K251795. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is a medical device that received FDA 510(k) clearance on 2025-10-09. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K251795.

When did Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) receive FDA 510(k) clearance?

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) received FDA 510(k) clearance on 2025-10-09, under 510(k) number K251795.

Who is the listed applicant for Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

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 Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

The FDA product code for Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is DXN.

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Otros registros que enlistan a Honsun (Nantong) Co., Ltd. como solicitante

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Dispositivos relacionados (Código: DXN)

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Fuente oficial

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