Medical Device Recalls
-
1 result found
510(K) Number: K140799 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) an... | 2 | 02/03/2017 | Angiodynamics Inc. (Navilyst Medical Inc.) |
-