510(k) K926157 ยท HQZ Frame, Spectacle
EYEGLASS FRAME
| Applicant | Roi Factory Direct Frame Co., Phoenix AR, US |
| Decision | Substantially Equivalent, May 6, 1993 |
| Received | Dec 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926157
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.