meddevicedb.com FDA Device Reference

SENSORY ROLLER MASSAGER

K833090 Class I Traditional
Decision Date
1983-10-14
Sponsor / Applicant
Maddak, Inc.

Technical Specification

510(k) Submission ID K833090
Product Code ISA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1983-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SENSORY ROLLER MASSAGER received FDA 510(k) clearance under submission number K833090, sponsored by Maddak, 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 1983-10-14.

Classification & Regulation

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