Medical Device Recalls
-
1 result found
510(K) Number: K932166 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM, Silicone, Sterile- to ventilate the middle ear subseq... | 2 | 02/07/2024 | Olympus Corporation of the Americas |
-