Breathe Technologies is one of 18347 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Breathe Technologies - FDA 510(k) Cleared Devices
Recent clearances: Breathe Technologies Life2000™ Ventilation System, BREATHE TECHNOLOGIES LIFE2000 VENTILATION SYSTEM, BREATHE NIOV VENTILATION SYSTEM
3
Total
3
Cleared
0
Denied
Breathe Technologies has 3 FDA 510(k) cleared medical devices. Based in Alameda, US.
Historical record: 3 cleared submissions from 2014 to 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Breathe Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Coombs Medical Device Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Breathe Technologies
3 devices