Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K940581 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BagEasy manual resuscitation devices are used for patients requiring complete or intermittent ventil... | 1 | 09/08/2010 | Westmed Inc |
BagEasy manual resuscitation devices are used for patients requiring complete or intermittent ventil... | 1 | 09/08/2010 | Westmed Inc |
-