Jostra AG
Jostra AG holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2004.
Top product codes for Jostra AG
Recent clearances by Jostra AG
- K020983 — JOSTRA SUCKERS, MODEL JS
- K030264 — QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030
- K020784 — JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS
- K023132 — JOSTRA MECC SYSTEM
- K022022 — JOSTRA VENT CATHETERS, MODELS LV & HKV
- K020515 — JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA
- K014303 — JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE
- K013944 — JOSTRA DUAL STAGE VENOUS RETURN CANNULAE
- K013939 — JOSTRA FLOWPROBE FP-32E
- K012774 — JOSTRA ARTERIAL PERFUSION CANNULAE
- K012617 — JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A...
- K003551 — VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201
- K002857 — ELS CANNULA (KIT), MODEL M1210-88,M1510-88
Data sourced from openFDA. This site is unofficial and independent of the FDA.