510(k) K861705 ยท FTC Light, Ultraviolet, Dermatological
CORONA 3000 (DERMATOLOGIC ULTRAVIOLET LAMP)
| Applicant | Vita-Tan Corp., Kansas City MO, US |
| Decision | Substantially Equivalent, May 16, 1986 |
| Received | May 5, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861705
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.