510(k) K173392 ยท FDF Colonoscope And Accessories, Flexible/Rigid
Pure-Vu System
| Applicant | Motus GI Medical Technologies , Ltd., Tirat Carmel, IL |
| Decision | Substantially Equivalent, Dec 12, 2017 |
| Received | Oct 30, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173392
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.