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OASYS-ORAL AIRWAY SYSTEM

K030440 Class II Abbreviated
Decision Date
2003-08-26
Sponsor / Applicant
Mark Abramson, D.D.S., Inc.

Technical Specification

510(k) Submission ID K030440
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2003-08-26
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OASYS-ORAL AIRWAY SYSTEM received FDA 510(k) clearance under submission number K030440, sponsored by Mark Abramson, D.D.S., Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-08-26.

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.