Respironics California, Inc. is one of 18330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respironics California, Inc. - FDA 510(k) Cleared Devices
Recent clearances: V200 VENTILATOR WITH APRV MODE, ESPRIT VENTILATOR WITH APRV MODE, V200 INTELLI-TRAK OPTION, V200 VENTILATOR
11
Total
11
Cleared
0
Denied
Respironics California, Inc. has 11 FDA 510(k) cleared anesthesiology devices. Based in Carlsbad, US.
Historical record: 11 cleared submissions from 2002 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Respironics California, Inc.
11 devices
Cleared
Jan 13, 2012
V200 VENTILATOR WITH APRV MODE, ESPRIT VENTILATOR WITH APRV MODE
Anesthesiology
367d
Cleared
Aug 19, 2011
V200 INTELLI-TRAK OPTION
Anesthesiology
150d
Cleared
Dec 22, 2010
V200 VENTILATOR
Anesthesiology
153d
Cleared
Jan 09, 2009
V60 VENTILATOR, MODEL V8000
Anesthesiology
119d
Cleared
Dec 12, 2007
ESPRIT VENTILATOR AUTO-TRAK SENSITIVITY OPTION, MODEL V1000
Anesthesiology
103d
Cleared
Jul 30, 2007
ESPRIT VENTILATOR SPEAKING MODE OPTION, MODEL V1000
Anesthesiology
90d
Cleared
Jul 08, 2005
ESPRIT VENTILATOR NEONATAL OPTION, MODEL V1000
Anesthesiology
53d
Cleared
Jun 18, 2004
ESPRIT VENTILATOR WITH NICO-ESPRIT INTERFACE OPTION, MODEL V1000
Anesthesiology
22d
Cleared
Mar 16, 2004
PLV CONTINUUM VENTILATOR, MODEL P2000
Anesthesiology
78d
Cleared
Nov 20, 2003
PLV CONTINUUM VENTILATOR, MODEL P1000
Anesthesiology
458d
Cleared
Nov 06, 2002
ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS
Anesthesiology
30d