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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 9 of 9 Results
ProductCode: DWF Applicant: JOSTRA AG Decision Date To: 12/22/2014
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jostra suckers, model js jostra ag K020983 01/30/2004
jostra single stage venous return cathet jostra ag K020784 01/09/2003
jostra vent catheters, models lv & hkv jostra ag K022022 09/11/2002
jostra antegrade cardioplegia cannula jostra ag K020515 04/24/2002
jostra retrograde cardioplegia cannulae jostra ag K014303 03/26/2002
jostra dual stage venous return cannulae jostra ag K013944 02/11/2002
jostra arterial perfusion cannulae jostra ag K012774 11/16/2001
jostra arterial perfusion cannulae, mode jostra ag K012617 11/06/2001
els cannula (kit), model m1210-88,m1510- jostra ag K002857 10/05/2000
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