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FDA 510(k)

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

K-Number: K251795 · 2025-10-09

Decision Date2025-10-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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

When was Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) approved by the FDA?

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

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

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is manufactured by Honsun (Nantong) Co., Ltd..

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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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.