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FDA 510(k), K122501, AEI DR. TERAUCHI ULTRASONIC TIPS
FDA 510(k), K122501, AEI DR. TERAUCHI ULTRASONIC TIPS
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510(K) Number: K122501
Device Name: AEI DR. TERAUCHI ULTRASONIC TIPS
Manufacturer: AMERICAN EAGLE INSTRUMENTS, INC.
Device Classification Name: scaler, ultrasonic
Regulation Number: 872.4850
Classification Product Code: ELC
Date Received: 08/16/2012
Decision Date: 03/29/2013
Regulation Medical Specialty: Dental
Device Name: AEI DR. TERAUCHI ULTRASONIC TIPS
Manufacturer: AMERICAN EAGLE INSTRUMENTS, INC.
Device Classification Name: scaler, ultrasonic
Regulation Number: 872.4850
Classification Product Code: ELC
Date Received: 08/16/2012
Decision Date: 03/29/2013
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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