Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)
K-Number: K251795 · 2025-10-09
Device Summary
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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Related PubMed Literature
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.