Monebo Technologies, Inc. is one of 23688 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monebo Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDIOBELT ELECTRODE BELT, MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0, MONEBO AUTOMATIC ARRHYTHMIA DETECTION SOFTWARE LIBRARY, VERSION 1
3
Total
3
Cleared
0
Denied
Monebo Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 3 cleared submissions from 2005 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Monebo Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Monebo Technologies, Inc.
3 devices