510(k) K070622 ยท FDF Colonoscope And Accessories, Flexible/Rigid
NEOGUIDE ENDOSCOPY SYSTEM
| Applicant | Neoguide Systems, Inc., Los Gatos CA, US |
| Decision | Substantially Equivalent, Aug 14, 2007 |
| Received | Mar 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070622
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.