510(k) K252183 ยท KNW Instrument, Biopsy
Resitu Slider 09 (RESL09)
| Applicant | Resitu Medical AB, Uppsala, SE |
| Decision | Substantially Equivalent, Sep 24, 2025 |
| Received | Jul 11, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252183
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.