meddevicedb.com FDA Device Reference

Flexi-Seal PROTECT PLUS Fecal Management System (with ENFit Connector)

K190114 Class II Traditional
Decision Date
2019-04-30
Sponsor / Applicant
Convatec Limited

Technical Specification

510(k) Submission ID K190114
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2019-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Flexi-Seal PROTECT PLUS Fecal Management System (with ENFit Connector) received FDA 510(k) clearance under submission number K190114, sponsored by Convatec Limited. 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 2019-04-30.

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.