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AMSURE URETHRAL CATHETERIZATION TRAY

K030712 Class II Traditional
Decision Date
2003-05-23
Sponsor / Applicant
Amsino International, Inc.

Technical Specification

510(k) Submission ID K030712
Product Code FCM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2003-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMSURE URETHRAL CATHETERIZATION TRAY received FDA 510(k) clearance under submission number K030712, sponsored by Amsino International, 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 2003-05-23.

Classification & Regulation

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