510(k) K190126 ยท DQO Catheter, Intravascular, Diagnostic
Bendit2.7 Steerable Microcatheter
| Applicant | Bend IT Technologies, Ltd., Petach Tikva, IL |
| Decision | Substantially Equivalent, Aug 22, 2019 |
| Received | Jan 28, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190126
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.