meddevicedb.com FDA Device Reference

Enteral Feeding Catheter

K202748 Class II Traditional
Decision Date
2021-04-09
Sponsor / Applicant
Medcaptain Life Science Co., Ltd.

Technical Specification

510(k) Submission ID K202748
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2021-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Enteral Feeding Catheter received FDA 510(k) clearance under submission number K202748, sponsored by Medcaptain Life Science Co., Ltd.. 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 2021-04-09.

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.