510(k) K071218 ยท FST Light, Surgical, Fiberoptic
PROXENON 350, MODEL 902XX
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Jun 14, 2007 |
| Received | May 2, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071218
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.