510(k) K980197 ยท HQD Lens, Contact (Other Material) - Daily
ULTRACON/ULTRACON S RIGID GAS PERMEABLE CONTACT LENS FOR DAILY WEAR
| Applicant | Specialty Ultravision, Inc., Campbell CA, US |
| Decision | Substantially Equivalent, Aug 4, 1998 |
| Received | Jan 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980197
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.