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RS2MI MUSCLE STIMULATOR FAMILY

K021763 Class II Traditional
Decision Date
2002-06-13
Sponsor / Applicant
Rs Medical

Technical Specification

510(k) Submission ID K021763
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2002-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RS2MI MUSCLE STIMULATOR FAMILY received FDA 510(k) clearance under submission number K021763, sponsored by Rs Medical. 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 2002-06-13.

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.