meddevicedb.com FDA Device Reference

RT Carbon ECG Leads

K240087 Class II Traditional
Decision Date
2024-09-13
Sponsor / Applicant
Ivy Biomedical Systems, Inc.

Technical Specification

510(k) Submission ID K240087
Product Code DSA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2900
Decision Date 2024-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RT Carbon ECG Leads received FDA 510(k) clearance under submission number K240087, sponsored by Ivy Biomedical Systems, 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 2024-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code DSA and 21 CFR 870.2900, within the Cardiovascular review panel as a Class II device.