Hmicro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hmicro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)
2
Total
2
Cleared
0
Denied
Hmicro, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Altos, US.
Historical record: 2 cleared submissions from 2014 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hmicro, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lifesignals, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hmicro, Inc.
2 devices