510(k) K827890 ยท FTC Light, Ultraviolet, Dermatological
FOLDALITE UNIT
| Applicant | National Biological Corp., Twinsburg OH, US |
| Decision | Substantially Equivalent, Aug 23, 1982 |
| Received | Aug 11, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K827890
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.