510(k) K071664 ยท QEY Mechanical Thrombolysis Catheter
TRELLIS-6 PERIPHERAL INFUSION SYSTEM
| Applicant | Bacchus Vascular, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 13, 2007 |
| Received | Jun 18, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071664
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 2, 2015 | Medtronic Inc. Cardiac Rhythm Disease Management Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, Terminated |
KRA | None listed |
| Feb 3, 2015 | Covidien Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO.
Product Usage: Intended for controlled and selective infusion of physic Terminated |
KRA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.