510(k) K210734 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
Endovascular Dilator and Sets
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Apr 6, 2021 |
| Received | Mar 11, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210734
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.