Medical Device Recalls
-
1 result found
510(K) Number: K110474 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Philips IntelliVue TcG10; Monitor, carbon-dioxide, cutaneous. The IntelliVue TcG10 is a device fo... | 2 | 01/16/2015 | Philips Medical Systems, Inc. |
-