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FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE

K102548 Class II Traditional
Decision Date
2010-11-26
Sponsor / Applicant
Footprint Medical, Inc.

Technical Specification

510(k) Submission ID K102548
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2010-11-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE received FDA 510(k) clearance under submission number K102548, sponsored by Footprint Medical, 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 2010-11-26.

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.