510(k) K991780 ยท HQD Lens, Contact (Other Material) - Daily
FLUOREX 700 -UV (FLUSILFOCON A), FLUOREX 500-UV (FLUSILFOCON B) AND FLUOREX 300-UV (FLUSILFOCON C) RIGID GAS PERMEABLE C
| Applicant | G.T. Laboratories, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jun 29, 1999 |
| Received | May 25, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991780
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.