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 7 of 7 Results
ProductCode: KRA Applicant: BACCHUS VASCULAR, INC. Decision Date To: 05/04/2024
Results per Page
New Search  
Export all 7 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]
spiralfuse peripheral infusion system BACCHUS VASCULAR, INC. K082199 10/17/2008
trellis-6 peripheral infusion system BACCHUS VASCULAR, INC. K071664 07/13/2007
trellis-8 peripheral infusion system BACCHUS VASCULAR, INC. K050147 02/03/2005
trellis reserve infusion system BACCHUS VASCULAR, INC. K032261 08/22/2003
trellis-6 peripheral infusion system (140cm catheter length 10cm infusion length) BACCHUS VASCULAR, INC. K023514 12/02/2002
trellis plus infusion system (140cm catheter length 10cm infusion length 20cm (100cm catheter length 10cm infusion h BACCHUS VASCULAR, INC. K021958 07/03/2002
trellis infusion system (10cm infusion length); trellis infusion system (20cm infusion length) BACCHUS VASCULAR, INC. K013635 02/11/2002
-
-