K253751
- 510(k) number
- K253751
- Device name
- CXRDetectAI
- Applicant
- Neurocareai, Inc. (Dba Savelife.Ai) TX · US
- Product code
- QFM — Radiological Computer-Assisted Prioritization Softwa
- Decision date
- 2026-07-08
- Date received
- 2025-11-25
- 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: K253751.pdf
Official FDA record: K253751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.