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CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP

K821906 Class II Traditional
Decision Date
1982-07-13
Sponsor / Applicant
Corpak Medsystems

Technical Specification

510(k) Submission ID K821906
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1982-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP received FDA 510(k) clearance under submission number K821906, sponsored by Corpak Medsystems. 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 1982-07-13.

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.