meddevicedb.com FDA Device Reference

POWERPLAY MUSCLE MASSAGER

K122154 Class II Traditional
Decision Date
2012-11-21
Sponsor / Applicant
Fig, LLC

Technical Specification

510(k) Submission ID K122154
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2012-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWERPLAY MUSCLE MASSAGER received FDA 510(k) clearance under submission number K122154, sponsored by Fig, LLC. 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 2012-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.