meddevicedb.com FDA Device Reference

IN TEN-S

K011492 Class II Traditional
Decision Date
2001-07-05
Sponsor / Applicant
Ivoclar North America, Inc.

Technical Specification

510(k) Submission ID K011492
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2001-07-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IN TEN-S received FDA 510(k) clearance under submission number K011492, sponsored by Ivoclar North America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-07-05.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.