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HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5

K971442 Class II Traditional
Decision Date
1998-01-08
Sponsor / Applicant
Humed, Inc.

Technical Specification

510(k) Submission ID K971442
Product Code KPN
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.2040
Decision Date 1998-01-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5 received FDA 510(k) clearance under submission number K971442, sponsored by Humed, Inc.. 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 1998-01-08.

Classification & Regulation

This clearance is catalogued under FDA product code KPN and 21 CFR 876.2040, within the Gastroenterology, Urology review panel as a Class II device.