K252261
- 510(k) number
- K252261
- Device name
- InferCare RECIST
- Applicant
- Beijing Infervision Healthcare Medical Technology Co., Ltd. CN
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2026-03-13
- Date received
- 2025-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.8 MB · U.S. public domain
Also available from FDA: K252261.pdf
Official FDA record: K252261
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.