Medical Device Recalls
-
1 result found
510(K) Number: K983566 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
24mm Rotating C-Mount Coupler, Model Number 1088-020-121S2. The device in indicated for use in gene... | 2 | 08/24/2008 | Stryker Endoscopy |
-