Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K954311 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
The Ultem Polymeric Resin Koh Cup is a non- sterile, reusable vaginal fornices delineator. It is mad... | 2 | 05/26/2021 | CooperSurgical, Inc. |
Colpo-Pneumo Occluder, Part CPO-6 | 2 | 10/11/2018 | CooperSurgical, Inc. |
-