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IYUNNI 3ID TRI-FUNNEL FEEDING TUBE KIT

K100173 Class II Traditional
Decision Date
2010-04-16
Sponsor / Applicant
Sainath Intellectual Properties, LLC

Technical Specification

510(k) Submission ID K100173
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2010-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IYUNNI 3ID TRI-FUNNEL FEEDING TUBE KIT received FDA 510(k) clearance under submission number K100173, sponsored by Sainath Intellectual Properties, LLC. 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 2010-04-16.

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.