Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K053462 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Radio used in the Precess MRI Patient Monitoring System. 3160 (Precess) and HE97B, 94044, 94045 (ra... | 2 | 10/27/2011 |
FEI # 1051786 Invivo Corporation |
| 3.7 V Li-Polymer Battery, used in Precess MRI Compatible Patient Monitoring System and Achieva, Inte... | 2 | 02/06/2009 |
FEI # 1051786 Invivo Corporation |
-







