510(k) K073503 ยท FTC Light, Ultraviolet, Dermatological
VERSA LITE
| Applicant | Diomedics, Inc., Laguna Niguel CA, US |
| Decision | Substantially Equivalent, Jan 23, 2008 |
| Received | Dec 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073503
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.