Medical Device Recalls
-
1 result found
510(K) Number: K983069 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
DuoDiagnost, model 707015, Universal RF system Product Usage: is a mult-functional diagnostic X-... | 2 | 03/16/2012 | Philips Healthcare Inc. |
-