Medical Device Recalls
-
1 result found
510(K) Number: K091068 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SmarTemp Probe Covers with the Accutorr V Monitor; Rx only. Mindray DS USA, Inc. Mahway, NJ 07430.... | 2 | 04/15/2010 | Mindray DS USA, Inc., dba Datascope Patient Monitoring |
-