Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K945379 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Platinum Plus" LT , REF 46-601, UPN M001466010, LT/0.018/180, Sterilized with ethylene oxide gas, R... | 3 | 10/02/2008 |
FEI # 3002095335 Boston Scientific Corporation |
| Platinum Plus" LT , REF 46-602, UPN M001466020, LT/0.018/260, Sterilized with ethylene oxide gas, R... | 3 | 10/02/2008 |
FEI # 3002095335 Boston Scientific Corporation |
-







