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PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM

K023906 Class II Traditional
Decision Date
2003-02-19
Sponsor / Applicant
The Prometheus Group

Technical Specification

510(k) Submission ID K023906
Product Code KPI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5320
Decision Date 2003-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM received FDA 510(k) clearance under submission number K023906, sponsored by The Prometheus Group. 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 2003-02-19.

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.