510(k) K173365 ยท LRX Case, Contact Lens
Bausch + Lomb Boston Scleral Lens Case
| Applicant | Bausch & Lomb, Incorporated, Rochester NY, US |
| Decision | Substantially Equivalent, Nov 17, 2017 |
| Received | Oct 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173365
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.