510(k) K183032 ยท FDA Enteroscope And Accessories
FUJIFILM Double Balloon Endoscope EI580BT
| Applicant | Fujifilm Corporation, Ashigara Kami-Gun, JP |
| Decision | Substantially Equivalent, Jun 24, 2019 |
| Received | Nov 1, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183032
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.