K260588
- 510(k) number
- K260588
- Device name
- Cleerly LABS
- Applicant
- Cleerly, Inc. CO · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-07-29
- Date received
- 2026-02-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K260588.pdf
Official FDA record: K260588
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.