510(k) K930561 ยท HQZ Frame, Spectacle
SOLSTAR BRILLENMODE SPECTACLE FRAMES
| Applicant | Solstar Produktions GmbH, Austria, AT |
| Decision | Substantially Equivalent, May 3, 1993 |
| Received | Feb 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930561
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.