meddevicedb.com FDA Device Reference

MODERN MEDICAL BIPOLAR FORCEPS

K032327 Class II Traditional
Decision Date
2004-06-15
Sponsor / Applicant
Modern Medical Equipment Mfg., Ltd.

Technical Specification

510(k) Submission ID K032327
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2004-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODERN MEDICAL BIPOLAR FORCEPS received FDA 510(k) clearance under submission number K032327, sponsored by Modern Medical Equipment Mfg., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-06-15.

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.