510(k) K232609 · DRE Dilator, Vessel, For Percutaneous Catheterization
Micro Ace Advanced Micro Access System
| Applicant | Merit Medical Systems, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Sep 27, 2023 |
| Received | Aug 28, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232609
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.