meddevicedb.com FDA Device Reference

Cardiac Guidance

K243065 Class II Traditional
Decision Date
2025-01-15
Sponsor / Applicant
Caption Health, Inc.

Technical Specification

510(k) Submission ID K243065
Product Code QJU
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2100
Decision Date 2025-01-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cardiac Guidance received FDA 510(k) clearance under submission number K243065, sponsored by Caption Health, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-01-15.

Classification & Regulation

This clearance is catalogued under FDA product code QJU and 21 CFR 892.2100, within the Radiology review panel as a Class II device.