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MYOTRAC INFINITI ELECTRICAL STIMULATOR

K053434 Class II Traditional
Decision Date
2006-03-15
Sponsor / Applicant
Thought Technology , Ltd.

Technical Specification

510(k) Submission ID K053434
Product Code KPI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5320
Decision Date 2006-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MYOTRAC INFINITI ELECTRICAL STIMULATOR received FDA 510(k) clearance under submission number K053434, sponsored by Thought Technology , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2006-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code KPI and 21 CFR 876.5320, within the Gastroenterology, Urology review panel as a Class II device.