meddevicedb.com FDA Device Reference

Empulse M90

K242327 Class II Traditional
Decision Date
2024-12-10
Sponsor / Applicant
Concourse Assistive Technology Pty, Ltd.

Technical Specification

510(k) Submission ID K242327
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2024-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Empulse M90 received FDA 510(k) clearance under submission number K242327, sponsored by Concourse Assistive Technology Pty, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2024-12-10.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.