Medical Device Recalls
-
1 result found
510(K) Number: K183266 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CardioTek EP-TRACER Software V2.x. | 2 | 06/23/2022 | CardioTek BV |
-