Medical Device Recalls
-
1 result found
510(K) Number: K993153 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Intralase FS Laser System. Laser Keratome | 2 | 08/12/2003 | Intralase Corp |
-