Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K013344 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System | 2 | 02/22/2019 | Philips Medical Systems Nederlands |
SENSE Body Coil 1.5T with identification; used in the ACS NT, Intera 1.5T and Achieva 1.5T MR syste... | 2 | 02/26/2016 | Philips Electronics North America Corporation |
-