510(k) K203842 ยท QJP Catheter, Percutaneous, Neurovasculature
Bendit21 Microcatheter
| Applicant | Bend IT Technologies, Ltd., Petach Tikva, IL |
| Decision | Substantially Equivalent, Apr 13, 2022 |
| Received | Dec 31, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203842
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.