Medical Device Manufacturer · US , Carlsbad , CA

Respironics California, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2002
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
1-11 of 11
Cleared Jan 13, 2012
V200 VENTILATOR WITH APRV MODE, ESPRIT VENTILATOR WITH APRV MODE
K110083 · CBK
Anesthesiology · 367d
Cleared Aug 19, 2011
V200 INTELLI-TRAK OPTION
K110795 · CBK
Anesthesiology · 150d
Cleared Dec 22, 2010
V200 VENTILATOR
K102054 · CBK
Anesthesiology · 153d
Cleared Jan 09, 2009
V60 VENTILATOR, MODEL V8000
K082660 · MNT
Anesthesiology · 119d
Cleared Dec 12, 2007
ESPRIT VENTILATOR AUTO-TRAK SENSITIVITY OPTION, MODEL V1000
K072450 · CBK
Anesthesiology · 103d
Cleared Jul 30, 2007
ESPRIT VENTILATOR SPEAKING MODE OPTION, MODEL V1000
K071212 · CBK
Anesthesiology · 90d
Cleared Jul 08, 2005
ESPRIT VENTILATOR NEONATAL OPTION, MODEL V1000
K051262 · CBK
Anesthesiology · 53d
Cleared Jun 18, 2004
ESPRIT VENTILATOR WITH NICO-ESPRIT INTERFACE OPTION, MODEL V1000
K041412 · CBK
Anesthesiology · 22d
Cleared Mar 16, 2004
PLV CONTINUUM VENTILATOR, MODEL P2000
K034032 · NOU
Anesthesiology · 78d
Cleared Nov 20, 2003
PLV CONTINUUM VENTILATOR, MODEL P1000
K022750 · NOU
Anesthesiology · 458d
Cleared Nov 06, 2002
ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS
K023350 · CBK
Anesthesiology · 30d
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