510(k) K932612 ยท HQZ Frame, Spectacle
DAELIM CORP. EYE WEAR MODEL
| Applicant | Daelim Corp., Miami FL, US |
| Decision | Substantially Equivalent, Apr 6, 1994 |
| Received | May 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932612
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.