Medical Device Recalls
-
|
1 result found
510(K) Number: K211401 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Pulsed Laser System (TFL-SLS). Inten... | 2 | 08/15/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
-







