Bacchus Vascular, Inc.
Bacchus Vascular, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2008.
Top product codes for Bacchus Vascular, Inc.
Recent clearances by Bacchus Vascular, Inc.
- K082199 — SPIRALFUSE PERIPHERAL INFUSION SYSTEM
- K071664 — TRELLIS-6 PERIPHERAL INFUSION SYSTEM
- K050147 — TRELLIS-8 PERIPHERAL INFUSION SYSTEM
- K033997 — SOLERA PLUS THROMBECTOMY CATHETER, 55 CM AND 110 CM, MODELS BAC SMG 007 055, BAC SMG 007 110
- K032261 — Trellis Reserve Infusion System
- K022640 — SOLERA MAGNUM THROMBECTOMY CATHETER, 55 CM, MODEL BAC SMG 007 055 & SOLERA MAGNUM THROMBECTOMY CATHETER, 110 CM
- K023514 — TRELLIS-6 PERIPHERAL INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH)
- K021958 — TRELLIS PLUS INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH 20CM (100CM CATHETER LENGTH 10CM INFUSION H
- K013635 — TRELLIS INFUSION SYSTEM (10CM INFUSION LENGTH); TRELLIS INFUSION SYSTEM (20CM INFUSION LENGTH)
- K003570 — BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755
Data sourced from openFDA. This site is unofficial and independent of the FDA.