510(k) K970019 ยท LPL Lenses, Soft Contact, Daily Wear
MENICON Z BIFOCAL DESIGN LENS/MENICON Z TRIFOCAL DESIGN LENS
| Applicant | Menicon U.S.A., Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 25, 1997 |
| Received | Jan 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970019
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.