510(k) K812521 ยท FTC Light, Ultraviolet, Dermatological
SUNTANNING DEVICE (SEPAR. FROM K812225)
| Applicant | Klafs Sunlight Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 2, 1981 |
| Received | Sep 2, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812521
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.