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CYCLOPAC CP100 TENS BANDAGE

K800576 Class II Traditional
Decision Date
1980-05-23
Sponsor / Applicant
Cyclotechnical Medical Indust., Inc.

Technical Specification

510(k) Submission ID K800576
Product Code GZJ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 1980-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CYCLOPAC CP100 TENS BANDAGE received FDA 510(k) clearance under submission number K800576, sponsored by Cyclotechnical Medical Indust., 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 1980-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code GZJ and 21 CFR 882.5890, within the Neurology review panel as a Class II device.