Medical Device Recalls
-
|
1 result found
510(K) Number: K140763 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endos... | 2 | 10/01/2015 |
FEI # 1000122656 US Endoscopy Group Inc |
-







