Medical Device Recalls
-
|
21 to 21 of 21 Results
510(K) Number: K093514 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging system. Product Usa... | 1 | 07/24/2013 |
FEI # 2126677 GE Healthcare, LLC |
-







