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URINARY DRAINAGE BAG

K935557 Class II Traditional
Decision Date
1994-03-07
Sponsor / Applicant
Puritas Health Care, Inc.

Technical Specification

510(k) Submission ID K935557
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1994-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URINARY DRAINAGE BAG received FDA 510(k) clearance under submission number K935557, sponsored by Puritas Health Care, 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 1994-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code KNX and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class II device.