meddevicedb.com FDA Device Reference

MC6A

K050735 Class II Traditional
Decision Date
2005-05-23
Sponsor / Applicant
Macan Engineering Co.

Technical Specification

510(k) Submission ID K050735
Product Code EKZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4920
Decision Date 2005-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MC6A received FDA 510(k) clearance under submission number K050735, sponsored by Macan Engineering Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code EKZ and 21 CFR 872.4920, within the Dental review panel as a Class II device.