Medical Device Recalls
-
1 result found
510(K) Number: K010787 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Permanent Pacing Lead (Catalog #: 03332, 03334, 03337, 03107, 03116, 03108, 03109, 05756, 53420, 057... | 2 | 09/24/2008 | Oscor, Inc. |
-