Medical Device Recalls
-
|
1 result found
510(K) Number: K914516 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies, America (OSTA); NTI Catalog N... | 2 | 03/24/2020 |
FEI # 1450997 Northgate Technologies, Inc. |
-







