meddevicedb.com FDA Device Reference

Pulp Canal Sealer, Pulp Canal Sealer EWT

K152956 Class II Traditional
Decision Date
2016-05-06
Sponsor / Applicant
Sybron Dental Specialties

Technical Specification

510(k) Submission ID K152956
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2016-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pulp Canal Sealer, Pulp Canal Sealer EWT received FDA 510(k) clearance under submission number K152956, 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 2016-05-06.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.