meddevicedb.com FDA Device Reference

Enteral Feeding Sets

K240039 Class II Traditional
Decision Date
2024-04-17
Sponsor / Applicant
Hangzhou Primecare Medical Co., Ltd.

Technical Specification

510(k) Submission ID K240039
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2024-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Enteral Feeding Sets received FDA 510(k) clearance under submission number K240039, sponsored by Hangzhou Primecare Medical 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 2024-04-17.

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.