510(k) K013762 ยท HQD Lens, Contact (Other Material) - Daily
RIGID GAS PERMEABLE CONTACT LENS
| Applicant | Bausch & Lomb, Incorporated, Rochester NY, US |
| Decision | Substantially Equivalent, Apr 3, 2002 |
| Received | Nov 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013762
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.