Medical Device Recalls
-
1 result found
510(K) Number: K113703 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A), Product Order Number Biotrue SVS - 7201, STERILE... | 2 | 11/04/2015 | Bausch & Lomb Inc Irb |
-