O-Two Medical Technologies, Inc. is one of 567 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
O-Two Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Equinox Advantage, O-TWO E700,O-TWO E600,O-TWO E500, EQUINOX RELIEVE
8
Total
8
Cleared
0
Denied
O-Two Medical Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Historical record: 8 cleared submissions from 2005 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by O-Two Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - O-Two Medical Technologies, Inc.
8 devices
Cleared
Aug 29, 2018
Equinox Advantage
Anesthesiology
331d
Cleared
Mar 16, 2015
O-TWO E700,O-TWO E600,O-TWO E500
Anesthesiology
276d
Cleared
Apr 30, 2012
EQUINOX RELIEVE
Anesthesiology
137d
Cleared
Dec 27, 2011
O_TWO CPAP SYSTEM
Anesthesiology
117d
Cleared
May 06, 2010
CAREVENT HANDHELD CPAP SYSTEM
Anesthesiology
140d
Cleared
Mar 06, 2009
CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR)
Anesthesiology
298d
Cleared
Sep 28, 2005
CAREVENT ATV+ AND CAREVENT MRI
Anesthesiology
117d
Cleared
Aug 30, 2005
CAREVENT CA AND DRA
Anesthesiology
49d