meddevicedb.com FDA Device Reference

Informed Vital Core Application (IVC App)

K241633 Class II Traditional
Decision Date
2024-11-18
Sponsor / Applicant
Mindset Medical, Inc.

Technical Specification

510(k) Submission ID K241633
Product Code QME
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2785
Decision Date 2024-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Informed Vital Core Application (IVC App) received FDA 510(k) clearance under submission number K241633, sponsored by Mindset Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code QME and 21 CFR 870.2785, within the Cardiovascular review panel as a Class II device.