Microlife Intellectual Property GmbH, Switzerland is one of 16091 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microlife Intellectual Property GmbH, Switzerland - FDA 510(k) Cleare...
Recent clearances: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Microlife Wrist Watch Blood Pressure Monitor, MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR
3
Total
3
Cleared
0
Denied
Microlife Intellectual Property GmbH, Switzerland has 3 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Microlife Intellectual Property GmbH, Switzerland Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microlife Intellectual Property GmbH, Switzerland
3 devices