meddevicedb.com FDA Device Reference

armor LC

K182118 Class I Traditional
Decision Date
2019-05-03
Sponsor / Applicant
Mavrik Dental Systems, Ltd.

Technical Specification

510(k) Submission ID K182118
Product Code EIE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6300
Decision Date 2019-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

armor LC received FDA 510(k) clearance under submission number K182118, sponsored by Mavrik Dental Systems, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code EIE and 21 CFR 872.6300, within the Dental review panel as a Class I device.