Medical Device Recalls
-
|
1 result found
510(K) Number: K160685 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF... | 2 | 04/29/2020 |
FEI # 2183461 WELCH ALLYN, INC/MORTARA |
-







