510(k) K833259 ยท HQG Lens, Spectacle, Non-Custom (Prescription)
MULTIPLE
| Applicant | Sun House Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 2, 1984 |
| Received | Sep 20, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833259
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.