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ENTERAL BAG/SET

K880051 Class II Traditional
Decision Date
1988-04-14
Sponsor / Applicant
Churchill Corp.

Technical Specification

510(k) Submission ID K880051
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1988-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENTERAL BAG/SET received FDA 510(k) clearance under submission number K880051, sponsored by Churchill Corp.. 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 1988-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code KNT and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.