meddevicedb.com FDA Device Reference

LONG TERM PERITONEAL CATHETER

K854614 Class II Traditional
Decision Date
1985-12-19
Sponsor / Applicant
Thermadics, Inc.

Technical Specification

510(k) Submission ID K854614
Product Code FJS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1985-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LONG TERM PERITONEAL CATHETER received FDA 510(k) clearance under submission number K854614, sponsored by Thermadics, 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 1985-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code FJS and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.