meddevicedb.com FDA Device Reference

ASD Oral Appliances

K163580 Class II Traditional
Decision Date
2017-06-08
Sponsor / Applicant
American Sleep Dentistry

Technical Specification

510(k) Submission ID K163580
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2017-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASD Oral Appliances received FDA 510(k) clearance under submission number K163580, sponsored by American Sleep Dentistry. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-06-08.

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.