meddevicedb.com FDA Device Reference

TRC-PEX, RADIC-SEALER

K132123 Class II Traditional
Decision Date
2014-03-20
Sponsor / Applicant
Km Corporation

Technical Specification

510(k) Submission ID K132123
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2014-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRC-PEX, RADIC-SEALER received FDA 510(k) clearance under submission number K132123, sponsored by Km Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-03-20.

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.