meddevicedb.com FDA Device Reference

CINA-ASPECTS

K233342 Class II Traditional
Decision Date
2024-03-15
Sponsor / Applicant
Avicenna.Ai

Technical Specification

510(k) Submission ID K233342
Product Code POK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2060
Decision Date 2024-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CINA-ASPECTS received FDA 510(k) clearance under submission number K233342, sponsored by Avicenna.Ai. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code POK and 21 CFR 892.2060, within the Radiology review panel as a Class II device.