meddevicedb.com FDA Device Reference

AGALLOY, DISALLOY, EPSILON AND LAMBDA

K942430 Class II Traditional
Decision Date
1994-07-14
Sponsor / Applicant
Fen Dental Mfg., Inc.

Technical Specification

510(k) Submission ID K942430
Product Code EJJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 1994-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AGALLOY, DISALLOY, EPSILON AND LAMBDA received FDA 510(k) clearance under submission number K942430, sponsored by Fen Dental Mfg., 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 1994-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code EJJ and 21 CFR 872.3070, within the Dental review panel as a Class II device.