meddevicedb.com FDA Device Reference

SERVICE MANAGER SM40SE

K053464 Class II Traditional
Decision Date
2006-06-06
Sponsor / Applicant
Conmed Integrated Systems, Canada, Ulc

Technical Specification

510(k) Submission ID K053464
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 2006-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERVICE MANAGER SM40SE received FDA 510(k) clearance under submission number K053464, sponsored by Conmed Integrated Systems, Canada, Ulc. 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 2006-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code FYD and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.