K252183 is an FDA 510(k) clearance for the Resitu Slider 09 (RESL09), a Instrument, Biopsy (Class II — Special Controls, product code KNW), submitted by Resitu Medical AB (Uppsala, SE). The FDA issued a Cleared decision on September 24, 2025, 75 days after receiving the submission on July 11, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1075.
| 510(k) Number | K252183 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 11, 2025 |
| Decision Date | September 24, 2025 |
| Days to Decision | 75 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | KNW — Instrument, Biopsy |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1075 |