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URINE METER, 250CC

K871042 Class II Traditional
Decision Date
1987-03-25
Sponsor / Applicant
Salt Creek Medical Technologies

Technical Specification

510(k) Submission ID K871042
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1987-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URINE METER, 250CC received FDA 510(k) clearance under submission number K871042, sponsored by Salt Creek Medical Technologies. 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 1987-03-25.

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.