510(k) K213773 ยท FDF Colonoscope And Accessories, Flexible/Rigid
Insufflation Retention Device
| Applicant | Bpendo, LLC, Norman OK, US |
| Decision | Substantially Equivalent, Jul 21, 2022 |
| Received | Dec 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213773
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.