510(k) K851039 ยท HQZ Frame, Spectacle
EYEDENTITY EYEWEAR
| Applicant | Vitech Research C/O Johnsen, Manfredi & Thorpe, Los Angeles CA, US |
| Decision | Substantially Equivalent, Apr 1, 1985 |
| Received | Mar 14, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851039
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.