Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i)
K-Number: K251307 · 2026-01-12
Decision Date2026-01-12
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) is a medical device manufactured by Shenzhen Hingmed Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2026-01-12 under approval number K251307. 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 Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i)?
Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) is a medical device that received FDA 510(k) clearance on 2026-01-12. It is manufactured by Shenzhen Hingmed Medical Instrument Co., Ltd.. The 510(k) number is K251307.
When was Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) approved by the FDA?
Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) received FDA 510(k) clearance on 2026-01-12, under approval number K251307.
What company makes Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i)?
Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) is manufactured by Shenzhen Hingmed Medical Instrument Co., Ltd..
What is the FDA product code for Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i)?
The FDA product code for Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) is DXN.
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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.