Medical Device Recalls
-
|
1 result found
510(K) Number: K020527 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| American Optisurgical, Horizon Phacoemulsification System, Model: HZN-2030, for ophthalmic surgery. | 2 | 09/04/2009 |
FEI # 1000135560 American Optisurgical Inc |
-







