TRELLIS-8 PERIPHERAL INFUSION SYSTEM— 510(k) K050147
Substantially EquivalentBacchus Vascular, Inc.
FDA 510(k) clearance K050147 for TRELLIS-8 PERIPHERAL INFUSION SYSTEM, Substantially Equivalent on 2005-02-03. Applicant: Bacchus Vascular, Inc.. Device class: 2.
Clearance details
- Applicant
- Bacchus Vascular, Inc.
- Product code
- Code QEY
- Device class
- Class 2
- Regulation
- 21 CFR 870.5150
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Santa Clara, CA, US
Recent devices under product code QEY
view all- K260149 — Versus Catheter (VS110-9NB)
- K251318 — VariFuse Adjustable Infusion Catheter
- K241851 — Versus Catheter (VS110-8B)
- K231653 — BASHIR .035 Endovascular Catheter, BASHIR S-B .035 Endovascular Catheter
- K222095 — BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101
More clearances from Bacchus Vascular, Inc.
view all- K082199 — SPIRALFUSE PERIPHERAL INFUSION SYSTEM
- K071664 — TRELLIS-6 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.