Jostra AG
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K020983 | JOSTRA SUCKERS, MODEL JS | DWF | 2004-01-30 | View |
| 510(k) | K030264 | QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030 | DTZ | 2003-02-26 | View |
| 510(k) | K020784 | JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS | DWF | 2003-01-09 | View |
| 510(k) | K023132 | JOSTRA MECC SYSTEM | KFM | 2002-12-17 | View |
| 510(k) | K022022 | JOSTRA VENT CATHETERS, MODELS LV & HKV | DWF | 2002-09-11 | View |
| 510(k) | K020515 | JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA | DWF | 2002-04-24 | View |
| 510(k) | K014303 | JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE | DWF | 2002-03-26 | View |
| 510(k) | K013944 | JOSTRA DUAL STAGE VENOUS RETURN CANNULAE | DWF | 2002-02-11 | View |
| 510(k) | K013939 | JOSTRA FLOWPROBE FP-32E | DPT | 2001-12-14 | View |
| 510(k) | K012774 | JOSTRA ARTERIAL PERFUSION CANNULAE | DWF | 2001-11-16 | View |
| 510(k) | K012617 | JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A... | DWF | 2001-11-06 | View |
| 510(k) | K003551 | VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201 | DTN | 2001-07-11 | View |
| 510(k) | K002857 | ELS CANNULA (KIT), MODEL M1210-88,M1510-88 | DWF | 2000-10-05 | View |
No matching devices.
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