Medical Device Recalls
-
1 result found
510(K) Number: K081800 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquisition and ... | 2 | 04/29/2020 | WELCH ALLYN, INC/MORTARA |
-