Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K180589 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
DR 800. Digital Radiography X-ray System. | 2 | 08/27/2024 | Agfa N.V. |
AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product U... | 2 | 06/03/2020 | Agfa N.V. |
AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 8... | 2 | 07/30/2019 | Agfa N.V. |
-