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BELZER UW-CSS

K883782 Class II Traditional
Decision Date
1989-04-20
Sponsor / Applicant
Du Pont Critical Care

Technical Specification

510(k) Submission ID K883782
Product Code KDL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5880
Decision Date 1989-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BELZER UW-CSS received FDA 510(k) clearance under submission number K883782, sponsored by Du Pont Critical Care. 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 1989-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code KDL and 21 CFR 876.5880, within the Gastroenterology, Urology review panel as a Class II device.