Pneupac , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: COMPPAC 200HD, PARAPAC 200D TRANSPORT, MODEL V200D, COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pneupac , Ltd. Anesthesiology ✕
15 devices
Cleared
May 27, 2004
COMPPAC 200HD
Anesthesiology
132d
Cleared
Sep 29, 2003
PARAPAC 200D TRANSPORT, MODEL V200D
Anesthesiology
200d
Cleared
Jul 17, 2003
COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER
Anesthesiology
407d
Cleared
Dec 13, 2002
PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200D
Anesthesiology
268d
Cleared
Oct 10, 1996
PARAPAC
Anesthesiology
248d
Cleared
Jan 12, 1987
PATIENT VALVE WITH AIR ENTRAINMENT
Anesthesiology
173d
Cleared
Oct 15, 1986
MODELS 2R AND 3R PNEUPAC VENTILATOR/RESUSCITATOR
Anesthesiology
84d
Cleared
Oct 04, 1984
PNEUPAC INSTANT ACTION VENTILATOR/RESUS
Anesthesiology
9d
Cleared
Nov 14, 1983
PNEU PAC VENTILATOR/RESUSCITATORS
Anesthesiology
96d
Cleared
Feb 18, 1982
VENTILATOR MODELS
Anesthesiology
22d
Cleared
Feb 05, 1980
PNEUPAC OXYGEN THERAPY UNIT
Anesthesiology
64d
Cleared
Feb 05, 1980
PNEUPAC VENTILATOR/RESUSCITATOR #2
Anesthesiology
64d
Cleared
Feb 05, 1980
PNEUPAC VENTILATOR/RESUSCITATOR #3
Anesthesiology
64d
Cleared
Feb 05, 1980
COMPRESSOR
Anesthesiology
64d
Cleared
Feb 05, 1980
PNEUPAC VENTILATOR/RESUSCITATOR
Anesthesiology
64d