meddevicedb.com FDA Device Reference

DeepHealth ProstateAI

K253682 Class II Traditional
Decision Date
2026-04-29
Sponsor / Applicant
Quantib B.V.

Technical Specification

510(k) Submission ID K253682
Product Code QDQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2090
Decision Date 2026-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DeepHealth ProstateAI received FDA 510(k) clearance under submission number K253682, sponsored by Quantib B.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code QDQ and 21 CFR 892.2090, within the Radiology review panel as a Class II device.