Medical Device Recalls
-
1 result found
510(K) Number: K940593 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses. | 2 | 06/14/2016 | Staar Surgical Co. |
-