meddevicedb.com FDA Device Reference

NEEDLELESS URINE SAMPLING PORT

K944236 Class II Traditional
Decision Date
1994-11-16
Sponsor / Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health

Technical Specification

510(k) Submission ID K944236
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1994-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEEDLELESS URINE SAMPLING PORT received FDA 510(k) clearance under submission number K944236, sponsored by Kendall Healthcare Products Co. Div.Of Tyco Health. 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 1994-11-16.

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.