Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K120638 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modali... | 2 | 10/22/2018 | Canon Medical System, USA, INC. |
MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan 3T MRI System Product Usage: MRI System. | 2 | 04/11/2013 | Toshiba American Medical Systems Inc |
-