FDA 510(k) Applications Submitted by BAUSCH & LOMB, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K173480 | 11/13/2017 | Crystalsert Lens Delivery System | Bausch & Lomb, Inc |
| K082132 | 07/29/2008 | BAUSCH & LOMB D4600A AIR EXCHANGE LINE PACK | BAUSCH & LOMB, INC |
| K192005 | 07/29/2019 | Bausch + Lomb PreVue Inserter for enVista Preloaded | Bausch & Lomb, Inc |
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