510(k) K850905 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
CR-39 TYPE RESIN
| Applicant | Orplex Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 20, 1985 |
| Received | Mar 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850905
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.