meddevicedb.com FDA Device Reference

ACCU-STAIN

K771887 Class II Traditional
Decision Date
1977-11-14
Sponsor / Applicant
Williams Gold Refining Co., Inc.

Technical Specification

510(k) Submission ID K771887
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1977-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCU-STAIN received FDA 510(k) clearance under submission number K771887, 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 1977-11-14.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.