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STERILE FOLEY CATHETERS & UROLOGICAL

K831743 Class II Traditional
Decision Date
1983-09-12
Sponsor / Applicant
Electromedics, Inc.

Technical Specification

510(k) Submission ID K831743
Product Code KOD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1983-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE FOLEY CATHETERS & UROLOGICAL received FDA 510(k) clearance under submission number K831743, sponsored by Electromedics, 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 1983-09-12.

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.