510(k) K171404 ยท HQD Lens, Contact (Other Material) - Daily
BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)
| Applicant | Bausch + Lomb, Incorporated, Rochester NY, US |
| Decision | Substantially Equivalent, Jul 17, 2017 |
| Received | May 12, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171404
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.