K253650
- 510(k) number
- K253650
- Device name
- Anura Mobile Core SDK (M1)
- Applicant
- Nuralogix Corporation CA
- Product code
- QME — Software For Optical Camera-Based Measurement Of Pul
- Decision date
- 2026-06-11
- Date received
- 2025-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253650.pdf
Official FDA record: K253650
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.