Medical Device Recalls
-
1 result found
510(K) Number: K143057 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 Int... | 2 | 02/28/2018 | Philips Electronics North America Corporation |
-