meddevicedb.com FDA Device Reference

FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH BUMPS)

K053065 Class II Traditional
Decision Date
2006-01-03
Sponsor / Applicant
Bryan Keropian Dds

Technical Specification

510(k) Submission ID K053065
Product Code LQZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2006-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH BUMPS) received FDA 510(k) clearance under submission number K053065, 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 2006-01-03.

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.