meddevicedb.com FDA Device Reference

URINARY DRAINAGE SET, CLOSED, STERILE

K770320 Class II Traditional
Decision Date
1977-03-16
Sponsor / Applicant
Medical Devices, Inc.

Technical Specification

510(k) Submission ID K770320
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1977-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URINARY DRAINAGE SET, CLOSED, STERILE received FDA 510(k) clearance under submission number K770320, sponsored by Medical Devices, 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 1977-03-16.

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.