Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K090512 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous... | 2 | 05/10/2021 | Bard Peripheral Vascular Inc |
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous... | 2 | 05/10/2021 | Bard Peripheral Vascular Inc |
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous... | 2 | 05/10/2021 | Bard Peripheral Vascular Inc |
-