meddevicedb.com FDA Device Reference

PMMA BLOCK

K141421 Class II Abbreviated
Decision Date
2015-02-09
Sponsor / Applicant
Rizhao Huge Dental Industry Co., Ltd.

Technical Specification

510(k) Submission ID K141421
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2015-02-09
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PMMA BLOCK received FDA 510(k) clearance under submission number K141421, sponsored by Rizhao Huge Dental Industry Co., Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-02-09.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.