510(k) K093037 ยท FDF Colonoscope And Accessories, Flexible/Rigid
PENTEX EC-3890LI
| Applicant | Pentax Medical Company, Montvale NJ, US |
| Decision | Substantially Equivalent, Dec 28, 2009 |
| Received | Sep 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093037
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.