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ASA ORAL APPLIANCES

K130504 Class II Traditional
Decision Date
2013-10-18
Sponsor / Applicant
American Sleep Association

Technical Specification

510(k) Submission ID K130504
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2013-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASA ORAL APPLIANCES received FDA 510(k) clearance under submission number K130504, sponsored by American Sleep Association. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-10-18.

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.