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RESTFUL NIGHTS, IST-APPLIANCE

K021569 Class II Traditional
Decision Date
2004-03-15
Sponsor / Applicant
Ottawa Dental Laboratory

Technical Specification

510(k) Submission ID K021569
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2004-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESTFUL NIGHTS, IST-APPLIANCE received FDA 510(k) clearance under submission number K021569, sponsored by Ottawa 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 2004-03-15.

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.