510(k) K950878 ยท LRX Case, Contact Lens
MENICON SP VIAL
| Applicant | Hyman, Phelps & McNamara, P.C., Washington Dc DC, US |
| Decision | Substantially Equivalent, Apr 7, 1995 |
| Received | Feb 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950878
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.