Oridion Capnography, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Oridion Capnography, Inc. has 5 FDA 510(k) cleared medical devices. Based in Jerusalem, IL.
Historical record: 5 cleared submissions from 2006 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Oridion Capnography, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jan 11, 2011
CAPNOSTREAM 20P WITH MASIMO SPO2 BOARD
Anesthesiology
181d
Cleared
May 12, 2010
CAPNOSTREAM20 WITH MICROMEDICO2 MODULE
Anesthesiology
134d
Cleared
Feb 06, 2009
CAPNOSTREAM20 WITH INTEGRATED PULMONARY INDEX
Anesthesiology
179d
Cleared
Oct 11, 2007
CAPNOSTREAM 20 WITH A2 ADAPTIVE AVERAGING SOFTWARE
Anesthesiology
56d
Cleared
May 04, 2006
CAPNOSTREAM20 TWO PARAMETER BEDSIDE MONITOR & CAPNOSTREAM10 ONE PARAMETER...
Anesthesiology
115d