510(k) K091783 ยท FDF Colonoscope And Accessories, Flexible/Rigid
THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM
| Applicant | Avantis Medical Systems, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jul 7, 2009 |
| Received | Jun 17, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091783
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.