Medical Device Recalls
-
|
11 to 11 of 11 Results
510(K) Number: K950419 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Model 8100 Series Medley Medication Safety System Pump Module | 2 | 03/03/2005 |
FEI # 3003879246 Alaris Medical Systems Inc |
-







