meddevicedb.com FDA Device Reference

BUILD-IT FR

K000211 Class II Traditional
Decision Date
2000-03-17
Sponsor / Applicant
Jeneric/Pentron, Inc.

Technical Specification

510(k) Submission ID K000211
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2000-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUILD-IT FR received FDA 510(k) clearance under submission number K000211, sponsored by Jeneric/Pentron, 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 2000-03-17.

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.