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URETHRAL CATHETERIZATION TRAYS

K801785 Class II Traditional
Decision Date
1980-10-21
Sponsor / Applicant
The Healthcare Group Laboratories, Inc.

Technical Specification

510(k) Submission ID K801785
Product Code KOD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1980-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URETHRAL CATHETERIZATION TRAYS received FDA 510(k) clearance under submission number K801785, sponsored by The Healthcare Group Laboratories, 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 1980-10-21.

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.