meddevicedb.com FDA Device Reference

PM830 ELECTRIC MASSAGER

K891394 Class I Traditional
Decision Date
1989-04-10
Sponsor / Applicant
Back IN Action, Inc.

Technical Specification

510(k) Submission ID K891394
Product Code ISA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 1989-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PM830 ELECTRIC MASSAGER received FDA 510(k) clearance under submission number K891394, sponsored by Back IN Action, 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 1989-04-10.

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.