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SOFTSEAL HSG CATHETER

K040238 Class II Traditional
Decision Date
2004-06-22
Sponsor / Applicant
Modern Medical Equipment Mfg., Ltd.

Technical Specification

510(k) Submission ID K040238
Product Code LKF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 2004-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOFTSEAL HSG CATHETER received FDA 510(k) clearance under submission number K040238, sponsored by Modern Medical Equipment Mfg., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2004-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code LKF and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.