Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K080175 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Datascope AS3000 Anesthesia System; Mindray, North America. The AS3000 Anesthesia Delivery Syste... | 2 | 04/08/2010 | Mindray DS USA, Inc., dba Datascope Patient Monitoring |
AS3000 Anesthesia Delivery System. Datascope Patient Monitoring; A Mindray Global Company. The ... | 2 | 12/05/2008 | Mindray DS USA, Inc., dba Datascope Patient Monitoring |
-