510(k) K791721 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
ULTRAVUE BLENDED BIFOCAL LENS
| Applicant | American Optical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 23, 1979 |
| Received | Aug 30, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791721
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.