Medical Device Recalls
-
|
1 result found
510(K) Number: K050232 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| RigiflexTM 11 Single-Use Achalasia Balloon Dilator, Material Number (UPN) M00554510 Product Usage... | 3 | 07/10/2013 | Boston Scientific Corporation |
-







