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AEI DR. TERAUCHI ULTRASONIC TIPS

K122501 Class II Traditional
Decision Date
2013-03-29
Sponsor / Applicant
American Eagle Instruments, Inc.

Technical Specification

510(k) Submission ID K122501
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2013-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AEI DR. TERAUCHI ULTRASONIC TIPS received FDA 510(k) clearance under submission number K122501, sponsored by American Eagle Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.