Medical Device Recalls
-
1 result found
510(K) Number: K081826 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Intelligent 60mm Articulating Endoscopic Linear Cutter, product code i60; Intelligent 60mm Articulat... | 2 | 11/23/2009 | Surgical Devices/Covidien |
-