meddevicedb.com FDA Device Reference

ALPHA BOND-RITE II(TM) OR BOND-RITE II(TM) 2-PASTE ADHEV

K942742 Class II Traditional
Decision Date
1994-08-29
Sponsor / Applicant
Wallace A. Erickson & Co.

Technical Specification

510(k) Submission ID K942742
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 1994-08-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA BOND-RITE II(TM) OR BOND-RITE II(TM) 2-PASTE ADHEV received FDA 510(k) clearance under submission number K942742, sponsored by Wallace A. Erickson & 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 1994-08-29.

Classification & Regulation

This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.