meddevicedb.com FDA Device Reference

TENS&EMS units (SM9109A, SM9109B)

K241509 Class II Traditional
Decision Date
2024-06-27
Sponsor / Applicant
Plexus Yoga, LLC Dba Chirp

Technical Specification

510(k) Submission ID K241509
Product Code NUH
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2024-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TENS&EMS units (SM9109A, SM9109B) received FDA 510(k) clearance under submission number K241509, sponsored by Plexus Yoga, LLC Dba Chirp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2024-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code NUH and 21 CFR 882.5890, within the Neurology review panel as a Class II device.