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NIR LAT MALE EXTERNAL CATHETER

K855209 Class II Traditional
Decision Date
1986-01-10
Sponsor / Applicant
Mali, Inc.

Technical Specification

510(k) Submission ID K855209
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1986-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIR LAT MALE EXTERNAL CATHETER received FDA 510(k) clearance under submission number K855209, sponsored by Mali, 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 1986-01-10.

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.