Medical Device Recalls
-
|
1 result found
510(K) Number: K931009 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| IMPACT Catheters, Balloon Dilatation and Esophageal Dilatation Catheter, Model Number 307, STERILE, ... | 2 | 12/15/2009 |
FEI # 1318694 Numed Inc |
-







