meddevicedb.com FDA Device Reference

BriefCase-Triage: CARE Multi-triage CT Body

K252970 Class II Traditional
Decision Date
2026-01-07
Sponsor / Applicant
Aidoc Medical , Ltd.

Technical Specification

510(k) Submission ID K252970
Product Code QAS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2080
Decision Date 2026-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BriefCase-Triage: CARE Multi-triage CT Body received FDA 510(k) clearance under submission number K252970, sponsored by Aidoc Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code QAS and 21 CFR 892.2080, within the Radiology review panel as a Class II device.