Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)
K-Number: K222153 · 2023-02-03
ApplicantMicrolife Intellectual Property GmbH
Decision Date2023-02-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) is a medical device manufactured by Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2023-02-03 under approval number K222153. 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 Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)?
Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) is a medical device that received FDA 510(k) clearance on 2023-02-03. It is manufactured by Microlife Intellectual Property GmbH. The 510(k) number is K222153.
When was Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) approved by the FDA?
Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) received FDA 510(k) clearance on 2023-02-03, under approval number K222153.
What company makes Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)?
Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) is manufactured by Microlife Intellectual Property GmbH.
What is the FDA product code for Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)?
The FDA product code for Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR) 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.