meddevicedb.com FDA Device Reference

MMN-1 COARSE MANIPULATOR

K002653 Class II Traditional
Decision Date
2000-09-22
Sponsor / Applicant
Narishige Co., Ltd.

Technical Specification

510(k) Submission ID K002653
Product Code MQJ
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6150
Decision Date 2000-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MMN-1 COARSE MANIPULATOR received FDA 510(k) clearance under submission number K002653, sponsored by Narishige Co., 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 2000-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code MQJ and 21 CFR 884.6150, within the Obstetrics/Gynecology review panel as a Class II device.