meddevicedb.com FDA Device Reference

AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL

K863630 Class II Traditional
Decision Date
1987-03-11
Sponsor / Applicant
Austenal Dental, Inc.

Technical Specification

510(k) Submission ID K863630
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 1987-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL received FDA 510(k) clearance under submission number K863630, sponsored by Austenal Dental, 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 1987-03-11.

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.