Jostra AG
Jostra AG appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 30, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K020983 | JOSTRA SUCKERS, MODEL JS | January 30, 2004 |
| K031544 | HEATER COOLER UNIT, MODEL HCU 30 | August 7, 2003 |
| K030264 | QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030 | February 26, 2003 |
| K020784 | JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS | January 9, 2003 |
| K023132 | JOSTRA MECC SYSTEM | December 17, 2002 |
| K022022 | JOSTRA VENT CATHETERS, MODELS LV & HKV | September 11, 2002 |
| K020515 | JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA | April 24, 2002 |
| K014303 | JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE | March 26, 2002 |
| K013944 | JOSTRA DUAL STAGE VENOUS RETURN CANNULAE | February 11, 2002 |
| K013939 | JOSTRA FLOWPROBE FP-32E | December 14, 2001 |
| K012774 | JOSTRA ARTERIAL PERFUSION CANNULAE | November 16, 2001 |
| K012617 | JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A... | November 6, 2001 |
| K003551 | VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201 | July 11, 2001 |
| K002857 | ELS CANNULA (KIT), MODEL M1210-88,M1510-88 | October 5, 2000 |