Trellis Reserve Infusion System— 510(k) K032261
Substantially EquivalentBacchus Vascular, Inc.
FDA 510(k) clearance K032261 for Trellis Reserve Infusion System, Substantially Equivalent on 2003-08-22. 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
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More clearances from Bacchus Vascular, Inc.
view all- K082199 — SPIRALFUSE PERIPHERAL INFUSION SYSTEM
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- K033997 — SOLERA PLUS THROMBECTOMY CATHETER, 55 CM AND 110 CM, MODELS BAC SMG 007 055, BAC SMG 007 110
- 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.