meddevicedb.com FDA Device Reference

UNICRYL

K042288 Class II Traditional
Decision Date
2004-12-27
Sponsor / Applicant
United Medical Industries Co. , Ltd.

Technical Specification

510(k) Submission ID K042288
Product Code GAM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4493
Decision Date 2004-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNICRYL received FDA 510(k) clearance under submission number K042288, sponsored by United Medical Industries Co. , 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 2004-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code GAM and 21 CFR 878.4493, within the General, Plastic Surgery review panel as a Class II device.