510(k) K933891 ยท HQZ Frame, Spectacle
SPECTACLE FRAMES
| Applicant | Euro Frame Design, Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, Oct 18, 1993 |
| Received | Aug 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933891
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.