Jostra AG
13 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| JOSTRA SUCKERS, MODEL JS (K020983) | Jostra AG | 2004-01-30 |
| QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030 (K030264) | Jostra AG | 2003-02-26 |
| JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS (K020784) | Jostra AG | 2003-01-09 |
| JOSTRA MECC SYSTEM (K023132) | Jostra AG | 2002-12-17 |
| JOSTRA VENT CATHETERS, MODELS LV & HKV (K022022) | Jostra AG | 2002-09-11 |
| JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA (K020515) | Jostra AG | 2002-04-24 |
| JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE (K014303) | Jostra AG | 2002-03-26 |
| JOSTRA DUAL STAGE VENOUS RETURN CANNULAE (K013944) | Jostra AG | 2002-02-11 |
| JOSTRA FLOWPROBE FP-32E (K013939) | Jostra AG | 2001-12-14 |
| JOSTRA ARTERIAL PERFUSION CANNULAE (K012774) | Jostra AG | 2001-11-16 |
| JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A... (K012617) | Jostra AG | 2001-11-06 |
| VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201 (K003551) | Jostra AG | 2001-07-11 |
| ELS CANNULA (KIT), MODEL M1210-88,M1510-88 (K002857) | Jostra AG | 2000-10-05 |
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