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Jostra AG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020983JOSTRA SUCKERS, MODEL JSJanuary 30, 2004
K031544HEATER COOLER UNIT, MODEL HCU 30August 7, 2003
K030264QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030February 26, 2003
K020784JOSTRA SINGLE STAGE VENOUS RETURN CATHETERSJanuary 9, 2003
K023132JOSTRA MECC SYSTEMDecember 17, 2002
K022022JOSTRA VENT CATHETERS, MODELS LV & HKVSeptember 11, 2002
K020515JOSTRA ANTEGRADE CARDIOPLEGIA CANNULAApril 24, 2002
K014303JOSTRA RETROGRADE CARDIOPLEGIA CANNULAEMarch 26, 2002
K013944JOSTRA DUAL STAGE VENOUS RETURN CANNULAEFebruary 11, 2002
K013939JOSTRA FLOWPROBE FP-32EDecember 14, 2001
K012774JOSTRA ARTERIAL PERFUSION CANNULAENovember 16, 2001
K012617JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A...November 6, 2001
K003551VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201July 11, 2001
K002857ELS CANNULA (KIT), MODEL M1210-88,M1510-88October 5, 2000