FDA 510(k) Applications Submitted by BACCHUS VASCULAR, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K071664 06/18/2007 TRELLIS-6 PERIPHERAL INFUSION SYSTEM BACCHUS VASCULAR, INC.
K082199 08/04/2008 SPIRALFUSE PERIPHERAL INFUSION SYSTEM BACCHUS VASCULAR, INC.
K021958 06/14/2002 TRELLIS PLUS INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH 20CM (100CM CATHETER LENGTH 10CM INFUSION H BACCHUS VASCULAR, INC.
K013635 11/05/2001 TRELLIS INFUSION SYSTEM (10CM INFUSION LENGTH); TRELLIS INFUSION SYSTEM (20CM INFUSION LENGTH) BACCHUS VASCULAR, INC.
K032261 07/23/2003 Trellis Reserve Infusion System BACCHUS VASCULAR, INC.
K022640 08/08/2002 SOLERA MAGNUM THROMBECTOMY CATHETER, 55 CM, MODEL BAC SMG 007 055 & SOLERA MAGNUM THROMBECTOMY CATHETER, 110 CM BACCHUS VASCULAR, INC.
K023514 10/21/2002 TRELLIS-6 PERIPHERAL INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH) BACCHUS VASCULAR, INC.
K033997 12/24/2003 SOLERA PLUS THROMBECTOMY CATHETER, 55 CM AND 110 CM, MODELS BAC SMG 007 055, BAC SMG 007 110 BACCHUS VASCULAR, INC.
K050147 01/24/2005 TRELLIS-8 PERIPHERAL INFUSION SYSTEM BACCHUS VASCULAR, INC.
K003570 11/20/2000 BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755 BACCHUS VASCULAR, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact