meddevicedb.com FDA Device Reference

DISPOSABLE LAPAROSCOPIC INSTRUMENT

K070812 Class II Special
Decision Date
2007-09-14
Sponsor / Applicant
Modern Medical Equipment Mfg., Ltd.

Technical Specification

510(k) Submission ID K070812
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2007-09-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE LAPAROSCOPIC INSTRUMENT received FDA 510(k) clearance under submission number K070812, sponsored by Modern Medical Equipment Mfg., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2007-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.