meddevicedb.com FDA Device Reference

RELAX-A-TONE

K780436 Class II Traditional
Decision Date
1978-05-12
Sponsor / Applicant
Bio Response

Technical Specification

510(k) Submission ID K780436
Product Code HCC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5050
Decision Date 1978-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RELAX-A-TONE received FDA 510(k) clearance under submission number K780436, sponsored by Bio Response. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1978-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code HCC and 21 CFR 882.5050, within the Neurology review panel as a Class II device.