510(k) K873245 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
AR DIACOAT SINGLE VISION LENSES
| Applicant | Seiko Optical Products of America, Inc., Mahwah NJ, US |
| Decision | Substantially Equivalent, Oct 5, 1987 |
| Received | Aug 17, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873245
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.