Medical Device Recalls
-
1 result found
510(K) Number: K050614 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
GE Healthcare Muse v7 cardiology information system. Model number 2026443-001: MUSE 7.0 app cd, Mod... | 2 | 04/17/2013 | GE Healthcare, LLC |
-