meddevicedb.com FDA Device Reference

600/7 TO 600/288 VARIOUS TYPES OF AMER. PATTERN DE

K851711 Class I Traditional
Decision Date
1985-06-11
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851711
Product Code EMG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1985-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

600/7 TO 600/288 VARIOUS TYPES OF AMER. PATTERN DE received FDA 510(k) clearance under submission number K851711, sponsored by Artiberia. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1985-06-11.

Classification & Regulation

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