meddevicedb.com FDA Device Reference

LITECAST SOLDER

K780642 Class II Traditional
Decision Date
1978-05-03
Sponsor / Applicant
Williams Gold Refining Co., Inc.

Technical Specification

510(k) Submission ID K780642
Product Code EJH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3710
Decision Date 1978-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LITECAST SOLDER received FDA 510(k) clearance under submission number K780642, sponsored by Williams Gold Refining Co., 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 1978-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code EJH and 21 CFR 872.3710, within the Dental review panel as a Class II device.