Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K073542 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
GE OEC 9900 Elite GSP fluoroscopic x-ray system GE Healthcare, Surgery, Salt Lake City, UT. The sys... | 2 | 01/05/2009 | OEC Medical Systems, Inc |
GE OEC 9900 Elite ESP fluoroscopic x-ray system. GE Healthcare, Surgery, Salt Lake City, UT. The sys... | 2 | 01/05/2009 | OEC Medical Systems, Inc |
-