meddevicedb.com FDA Device Reference

FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSOR

K061228 Class II Traditional
Decision Date
2006-05-26
Sponsor / Applicant
Bryan Keropian Dds

Technical Specification

510(k) Submission ID K061228
Product Code LQZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2006-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSOR received FDA 510(k) clearance under submission number K061228, sponsored by Bryan Keropian Dds. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code LQZ and 21 CFR 872.5570, within the Dental review panel as a Class II device.