meddevicedb.com FDA Device Reference

THUMPER (VIBRATOR/MASSAGER)

K860159 Class I Traditional
Decision Date
1986-02-06
Sponsor / Applicant
Wellness Innovations Corp.

Technical Specification

510(k) Submission ID K860159
Product Code IRO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5975
Decision Date 1986-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THUMPER (VIBRATOR/MASSAGER) received FDA 510(k) clearance under submission number K860159, sponsored by Wellness Innovations Corp.. 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 1986-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code IRO and 21 CFR 890.5975, within the Physical Medicine review panel as a Class I device.