Medical Device Recalls
-
1 result found
510(K) Number: K981203 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, ... | 2 | 04/24/2014 | Teleflex Medical |
-