Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K952984 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA06100 Product Usage: Recommended for u... | 2 | 11/28/2018 |
FEI # 1318694 Numed Inc |
| Multi-Track Angiographic Catheter (MMTA) Product Code: MMTA05100 Product Usage: Recommended for u... | 2 | 11/28/2018 |
FEI # 1318694 Numed Inc |
-







