Medical Device Recalls
-
|
1 result found
510(K) Number: K946283 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Cepheid, Sample Collection Device, Part: 900-0370 | 2 | 08/14/2024 | Cepheid |
-







