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INNOVA COMFORTPULSE VAGINAL ELECTRODE (199204)/INNOVA COMFORTPULSE SMALL VAGINAL ELECTRODE(199205)

K964577 Class II Traditional
Decision Date
1997-01-24
Sponsor / Applicant
Empi

Technical Specification

510(k) Submission ID K964577
Product Code KPI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5320
Decision Date 1997-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INNOVA COMFORTPULSE VAGINAL ELECTRODE (199204)/INNOVA COMFORTPULSE SMALL VAGINAL ELECTRODE(199205) received FDA 510(k) clearance under submission number K964577, sponsored by Empi. 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 1997-01-24.

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.