Medical Device Recalls
-
|
1 result found
510(K) Number: K201798 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| myQA iON; Article Number: MQ10-000; | 2 | 04/30/2025 | IBA Dosimetry GmbH |
-







