meddevicedb.com FDA Device Reference

ARGYLE CLOSED URINARY DRAINAGE SET

K802667 Class II Traditional
Decision Date
1980-12-16
Sponsor / Applicant
Sherwood Medical Co.

Technical Specification

510(k) Submission ID K802667
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1980-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARGYLE CLOSED URINARY DRAINAGE SET received FDA 510(k) clearance under submission number K802667, sponsored by Sherwood Medical Co.. 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 1980-12-16.

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.