meddevicedb.com FDA Device Reference

1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS

K851724 Class I Traditional
Decision Date
1985-07-02
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851724
Product Code EKB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1985-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS received FDA 510(k) clearance under submission number K851724, 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 1985-07-02.

Classification & Regulation

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