meddevicedb.com FDA Device Reference

CATH-SECURE

K803062 Class II Traditional
Decision Date
1981-01-07
Sponsor / Applicant
Melissa C. Johnson

Technical Specification

510(k) Submission ID K803062
Product Code KOD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1981-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CATH-SECURE received FDA 510(k) clearance under submission number K803062, sponsored by Melissa C. Johnson. 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 1981-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code KOD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.