Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 9 of 9 Results
ProductCode: DWF Applicant: JOSTRA AG Decision Date To: 01/26/2015
Results per Page
New Search  
Export all 9 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
jostra suckers, model js JOSTRA AG K020983 01/30/2004
jostra single stage venous return catheters 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, model a... JOSTRA AG K012617 11/06/2001
els cannula (kit), model m1210-88,m1510-88 JOSTRA AG K002857 10/05/2000
-
-