Sensor Medics Corp. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Sensor Medics Corp. has 26 FDA 510(k) cleared anesthesiology devices. Based in Walker, US.
Historical record: 26 cleared submissions from 1984 to 2004.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
26 devices
Cleared
Mar 04, 2004
HIOX80 AEROSOL ADAPTER
Anesthesiology
203d
Cleared
Feb 13, 2004
INFANT FLOW PLUS INFANT CPAP SYSTEM WITH SIPAP FUNCTION
Anesthesiology
253d
Cleared
Aug 25, 2003
LYRA NASAL MASK
Anesthesiology
68d
Cleared
Apr 22, 2003
MODIFICATION TO HIOX
Anesthesiology
27d
Cleared
Jan 24, 2003
PEGASUS NASAL CPAP SYSTEM
Anesthesiology
203d
Cleared
Jul 30, 2002
HI-OX
Anesthesiology
151d
Cleared
Aug 02, 2001
SOMNO STAR & SERIES SLEEP SYSTEM
Neurology
30d
Cleared
Jul 24, 2001
MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT
Anesthesiology
25d
Cleared
Aug 13, 1999
INFANT FLOW SYSTEM
Anesthesiology
63d
Cleared
Feb 24, 1999
INFANT FLOW NCPAP MASKS
Anesthesiology
89d
Cleared
Oct 30, 1998
STATIC AND DYNAMIC COMPLIANCE, A RESPIRATORY MECHANICS OPTION FOR THE VMAX...
Anesthesiology
198d
Cleared
Jan 30, 1998
INFANT FLOW SYSTEM
Anesthesiology
74d