meddevicedb.com FDA Device Reference

COLORED WEDGE USED TO SEPARATE TEETH

K821444 Class I Traditional
Decision Date
1982-06-14
Sponsor / Applicant
Moyco Industries, Inc.

Technical Specification

510(k) Submission ID K821444
Product Code DZN
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1982-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COLORED WEDGE USED TO SEPARATE TEETH received FDA 510(k) clearance under submission number K821444, sponsored by Moyco Industries, 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 1982-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code DZN and 21 CFR 872.4565, within the Dental review panel as a Class I device.