meddevicedb.com FDA Device Reference

HEALTHY SLEEP APPLIANCE

K123410 Class II Traditional
Decision Date
2013-04-05
Sponsor / Applicant
Healthy Sleep Dental Laboratory

Technical Specification

510(k) Submission ID K123410
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2013-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEALTHY SLEEP APPLIANCE received FDA 510(k) clearance under submission number K123410, sponsored by Healthy Sleep Dental Laboratory. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-04-05.

Classification & Regulation

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