510(k) K864546 ยท FTC Light, Ultraviolet, Dermatological
MAXI-TAN DEVICE
| Applicant | National Biological Corp., Twinsburg OH, US |
| Decision | Substantially Equivalent, Jan 9, 1987 |
| Received | Nov 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864546
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.