Bacchus Vascular, Inc.
FDA 510(k) medical device clearances.
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.