510(k) K073423 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Dec 19, 2007 |
| Received | Dec 5, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K073423
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 1, 2019 | Bard Peripheral Vascular Inc 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With suture Plugs, (01)00801741026720;
2. PowerPort Implantable Port With Attachab Terminated |
LJT | None listed |
| Oct 1, 2019 | Bard Peripheral Vascular Inc 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ;
2. PowerPort M.R.I. Implantable Port with Terminated |
LJT | None listed |
| Oct 1, 2019 | Bard Peripheral Vascular Inc 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, Ref: 1809660, UDI: (01)00801741027154
2. PowerPort isp M.R.I. Implantable Por Terminated |
LJT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.