This page includes the latest FDA filings for Jostra Ag. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
JOSTRA AG | JOSTRA SUCKERS, MODEL JS | 2004-01-30 |
JOSTRA AG | QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030 | 2003-02-26 |
JOSTRA AG | JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS | 2003-01-09 |
JOSTRA AG | JOSTRA MECC SYSTEM | 2002-12-17 |
JOSTRA AG | JOSTRA VENT CATHETERS, MODELS LV & HKV | 2002-09-11 |
JOSTRA AG | JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA | 2002-04-24 |
JOSTRA AG | JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE | 2002-03-26 |
JOSTRA AG | JOSTRA DUAL STAGE VENOUS RETURN CANNULAE | 2002-02-11 |
JOSTRA AG | JOSTRA FLOWPROBE FP-32E | 2001-12-14 |
JOSTRA AG | JOSTRA ARTERIAL PERFUSION CANNULAE | 2001-11-16 |
JOSTRA AG | JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A... | 2001-11-06 |
JOSTRA AG | VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201 | 2001-07-11 |
JOSTRA AG | ELS CANNULA (KIT), MODEL M1210-88,M1510-88 | 2000-10-05 |