Medical Device Recalls
-
1 to 6 of 6 Results
510(K) Number: K945375 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ADVANTX LCA | 2 | 12/23/2016 | GE Healthcare, LLC |
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems... | 2 | 02/05/2016 | GE Medical Systems, LLC |
GE Healthcare, Advantx, Innova 2000, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova ... | 2 | 10/17/2013 | GE Healthcare, LLC |
Omega IV and Omega V tables on GE Advantx-E imaging system, used for general purpose diagnostic angi... | 2 | 01/13/2010 | GE Medical Systems, LLC |
Advantx-E The Advantx imaging system is intended to be used for general purpose diagnostic angiogra... | 2 | 09/21/2008 | GE Healthcare |
Advantx-E is an angiographic X-Ray system. | 2 | 09/16/2008 | GE Healthcare |
-