Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K122439 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383) | 2 | 05/31/2017 | Philips Electronics North America Corporation |
| Philips IntelliVue Monitors with software revisions J.21.03, J.21.19. Model Product MP5 M810... | 2 | 10/21/2014 | Philips Medical Systems, Inc. |
-







