510(k) K992787 ยท HQD Lens, Contact (Other Material) - Daily
EPICON (CARBOSILFOCON A) RIGID GAS PERMEABLE CONTACT LENS DAILY WEAR
| Applicant | Specialty Ultravision, Inc., Campbell CA, US |
| Decision | Substantially Equivalent, Feb 2, 2000 |
| Received | Aug 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992787
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.