510(k) K852403 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
AURALITE II
| Applicant | Aura Lens Products, St. Cloud MN, US |
| Decision | Substantially Equivalent, Aug 20, 1985 |
| Received | Jun 6, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852403
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.