meddevicedb.com FDA Device Reference

Life Fast Set, Life Regular Set

K150559 Class II Special
Decision Date
2015-06-19
Sponsor / Applicant
Sybron Dental Specialties

Technical Specification

510(k) Submission ID K150559
Product Code EJK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3250
Decision Date 2015-06-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Life Fast Set, Life Regular Set received FDA 510(k) clearance under submission number K150559, sponsored by Sybron Dental Specialties. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-06-19.

Classification & Regulation

This clearance is catalogued under FDA product code EJK and 21 CFR 872.3250, within the Dental review panel as a Class II device.