510(k) K860347 ยท FTC Light, Ultraviolet, Dermatological
SUNLAMP MODELS 24N, 30R, 30RE, 37RE
| Applicant | Gti, Inc., East Lyme CT, US |
| Decision | Substantially Equivalent, Feb 12, 1986 |
| Received | Jan 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860347
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.