ClearanceBrief
Company ยท US

Cardiopulmonary Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2013. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CBKVentilator, Continuous, Facility Use3
MSXSystem, Network And Communication, Physiological Monitors3
MODAccessory To Continuous Ventilator (Respirator)2
MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 20, 2013K130208BERNOULLI ENTERPRISE SOFTWARE
Cardiopulmonary Corp.
MHX
Aug 14, 2009K091461BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE
Cardiopulmonary Corp.
MOD
Sep 14, 2006K061932BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE
Cardiopulmonary Corp.
MSX
Jun 23, 2005K051283MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE
Cardiopulmonary Corp.
MSX
Feb 21, 2002K020018MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE
Cardiopulmonary Corp.
MSX
Nov 6, 2001K011861BERNOULLI VENTILATOR MANAGEMENT SYSTEM
Cardiopulmonary Corp.
MOD
Feb 24, 1999K990429MODIFICATION OF VENTURI VENTILATOR
Cardiopulmonary Corp.
CBK
Jun 24, 1998K982174VENTURI VENTILATOR
Cardiopulmonary Corp.
CBK
Oct 16, 1995K943412VENTURI VENTILATOR
Cardiopulmonary Corp.
CBK

Latest recalls

DateFirm and productCodeLinked 510(k)
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