Medical Device Recalls
-
|
1 result found
510(K) Number: K961940 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm redu... | 2 | 04/12/2023 |
FEI # 1219930 Covidien, LP |
-







