meddevicedb.com FDA Device Reference

BACK MASSAGER

K952043 Class I Traditional
Decision Date
1995-09-01
Sponsor / Applicant
Eight Corners, Inc.

Technical Specification

510(k) Submission ID K952043
Product Code LYG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1995-09-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACK MASSAGER received FDA 510(k) clearance under submission number K952043, sponsored by Eight Corners, Inc.. 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 1995-09-01.

Classification & Regulation

This clearance is catalogued under FDA product code LYG and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.