510(k) K090512 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Mar 27, 2009 |
| Received | Feb 26, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090512
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 25, 2021 | Bard Peripheral Vascular Inc PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for in Terminated |
LJT | None listed |
| Mar 25, 2021 | Bard Peripheral Vascular Inc PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829570, UDI: (01) 00801741027192 - Product Usage: The port system can be used for in Terminated |
LJT | None listed |
| Mar 25, 2021 | Bard Peripheral Vascular Inc PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 5829502, UDI: (01)00801741027406 - Product Usage: The port system can be used for inf Terminated |
LJT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.