meddevicedb.com FDA Device Reference

NEOMED POLYURETHANE FEEDING TUBE

K082238 Class II Special
Decision Date
2008-10-01
Sponsor / Applicant
Neomed, Inc.

Technical Specification

510(k) Submission ID K082238
Product Code FPD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2008-10-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEOMED POLYURETHANE FEEDING TUBE received FDA 510(k) clearance under submission number K082238, sponsored by Neomed, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2008-10-01.

Classification & Regulation

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