Medical Device Recalls
-
1 result found
510(K) Number: K871435 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catal... | 2 | 01/24/2013 | ConMed Corporation |
-