Medical Device Recalls
-
1 result found
510(K) Number: K193587 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. T... | 2 | 07/31/2020 | Sutter Medizintechnik GmbH |
-