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RELAXATION COURSE MODEL 1000

K770787 Class II Traditional
Decision Date
1977-06-17
Sponsor / Applicant
Cybernetic Medical, Inc.

Technical Specification

510(k) Submission ID K770787
Product Code HCC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5050
Decision Date 1977-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RELAXATION COURSE MODEL 1000 received FDA 510(k) clearance under submission number K770787, sponsored by Cybernetic Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1977-06-17.

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.