510(k) K862503 ยท HQZ Frame, Spectacle
KOELN OPTIK
| Applicant | South West Intl., Inc., Mobile AL, US |
| Decision | Substantially Equivalent, Jul 11, 1986 |
| Received | Jul 1, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862503
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.