46 results
·
64ms
·
Sources: EU EUDAMED, US FDA
PETITE PORT-A-CATH, 7 FR
FDA Adverse Event
Injury
·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·February 23, 1996
COOK PACEMAKER CORP. 115 UNIPOLAR CARDI
FDA 510(k)
FDA Class 3
·Cardiovascular
COOK PACEMAKER CORP. 116 BIOPOLAR CARDI
FDA 510(k)COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI
FDA 510(k)
FDA Class 3
·Cardiovascular
COOK PACEMAKER CORP. 332T BIPOLAR CARDIAC PULSE GE
FDA 510(k)
FDA Class 3
·Cardiovascular
VITAL PORT VASCULAR ACCESS SYSTEM
FDA Adverse Event
Injury
·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·December 28, 1995
BYRD DILATOR SHEATH SET TEFLON
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code GCC·September 23, 1996
VITAL PORT CATHETER
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code DQO·January 12, 1994
VITAL PORT
FDA Adverse Event
Other
·COOK PACEMAKER CORP.·Product code LJT·March 10, 1994
VITAL PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·February 7, 1995
VITAL PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LTH·February 13, 1995
VITAL-PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·February 1, 1995
VITAL PORT ACCESS SYSTEMS
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·January 19, 1995
COOK VITAL PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code DQO·October 26, 1994
VITAL PORT ACCESS DEVICE
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·June 26, 1997
VITAL-PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·November 8, 1996
VITAL-PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·November 13, 1996
VITAL-PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·December 6, 1996
VITAL-PORT
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·November 13, 1996
*
FDA Adverse Event
Injury
·COOK PACEMAKER CORP.·Product code LJT·October 23, 1996