K260300
- 510(k) number
- K260300
- Device name
- WatchMate Software
- Applicant
- Anumana, Inc. MA · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-06-15
- Date received
- 2026-01-30
- 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: K260300.pdf
Official FDA record: K260300
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.