meddevicedb.com FDA Device Reference

Nerve and Muscle Stimulator

K211094 Class II Traditional
Decision Date
2021-07-08
Sponsor / Applicant
Shenzhen Xft Medical Limited

Technical Specification

510(k) Submission ID K211094
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2021-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nerve and Muscle Stimulator received FDA 510(k) clearance under submission number K211094, sponsored by Shenzhen Xft Medical Limited. 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 2021-07-08.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.