Microlife Intellectual Property GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microlife Intellectual Property GmbH - FDA 510(k) Cleared Devices
Recent clearances: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K, Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5W, Microlife Upper Arm Automatic Digital BPM, Model WatchBP Office Vascular (TWIN200 VSR)
Microlife Intellectual Property GmbH has 54 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Last cleared in 2023. Active since 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Microlife Intellectual Property GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mdi Consultants, Inc. and Mdi Consutants, Inc..
FDA 510(k) Regulatory Record - Microlife Intellectual Property GmbH
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