Medical Device Manufacturer · US , Alameda , CA

Breathe Technologies - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014
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.

FDA 510(k) Regulatory Record - Breathe Technologies
3 devices
1-3 of 3
Cleared Aug 11, 2017
Breathe Technologies Life2000™ Ventilation System
K170037 · CBK
Anesthesiology · 219d
Cleared Jun 12, 2015
BREATHE TECHNOLOGIES LIFE2000 VENTILATION SYSTEM
K141943 · CBK
Anesthesiology · 330d
Cleared Mar 06, 2014
BREATHE NIOV VENTILATION SYSTEM
K131562 · ONZ
Anesthesiology · 280d
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