Full Automatic(NIBP) Blood Pressure Monitor
K-Number: K180240 · 2018-10-17
Device Summary
Frequently Asked Questions
What is the Full Automatic(NIBP) Blood Pressure Monitor?
Full Automatic(NIBP) Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2018-10-17. It is manufactured by Health & Life Co., Ltd.. The 510(k) number is K180240.
When was Full Automatic(NIBP) Blood Pressure Monitor approved by the FDA?
Full Automatic(NIBP) Blood Pressure Monitor received FDA 510(k) clearance on 2018-10-17, under approval number K180240.
What company makes Full Automatic(NIBP) Blood Pressure Monitor?
Full Automatic(NIBP) Blood Pressure Monitor is manufactured by Health & Life Co., Ltd..
What is the FDA product code for Full Automatic(NIBP) Blood Pressure Monitor?
The FDA product code for Full Automatic(NIBP) Blood Pressure Monitor is DXN.
Related Clinical Trials
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.