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HOSPIRA ENTERAL FEEDING SET, MODEL 20640

K061432 Class II Traditional
Decision Date
2006-09-11
Sponsor / Applicant
Hospira, Inc.

Technical Specification

510(k) Submission ID K061432
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2006-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOSPIRA ENTERAL FEEDING SET, MODEL 20640 received FDA 510(k) clearance under submission number K061432, sponsored by Hospira, 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 2006-09-11.

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.