K260500
- 510(k) number
- K260500
- Device name
- ResolutionMD
- Applicant
- ResolutionMD, Inc. CA
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-07-21
- Date received
- 2026-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K260500.pdf
Official FDA record: K260500
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.