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YAMAHACHI DENTURE BASE RESINS

K131036 Class II Traditional
Decision Date
2013-07-12
Sponsor / Applicant
Yamahachi Dental Manufacturing Co.

Technical Specification

510(k) Submission ID K131036
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2013-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YAMAHACHI DENTURE BASE RESINS received FDA 510(k) clearance under submission number K131036, sponsored by Yamahachi Dental Manufacturing Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.