meddevicedb.com FDA Device Reference

TAKE 1 ADVANCE

K130869 Class II Traditional
Decision Date
2013-05-30
Sponsor / Applicant
Sybron Dental Specialties

Technical Specification

510(k) Submission ID K130869
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2013-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAKE 1 ADVANCE received FDA 510(k) clearance under submission number K130869, sponsored by Sybron Dental Specialties. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-05-30.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.