Medical Device Recalls
-
1 result found
510(K) Number: K944495 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Devices includes a Multi Port Inflator or without Multi Port Inflator (MPI). All the devices are va... | 2 | 12/10/2012 | Parks Medical Electronics, Inc |
-