K260572
- 510(k) number
- K260572
- Device name
- Marrow Marxman
- Applicant
- Medimetrix, LLC TN · US
- Product code
- KNW — Instrument, Biopsy
- Decision date
- 2026-08-04
- Date received
- 2026-02-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K260572.pdf
Official FDA record: K260572
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.