510(k) K863518 ยท FTC Light, Ultraviolet, Dermatological
WEINGART MODEL 1000 SUNLAMP PRODUCT
| Applicant | Weingart, Inc., Ft Wayne IN, US |
| Decision | Substantially Equivalent, Oct 2, 1986 |
| Received | Sep 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863518
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.