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FDA 510(k), K820537, ULTRASONIC TOOTHBRUSH
FDA 510(k), K820537, ULTRASONIC TOOTHBRUSH
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510(K) Number: K820537
Device Name: ULTRASONIC TOOTHBRUSH
Manufacturer: ULTRASONIC PLAQUE CONTROL LABORATORIES
Device Classification Name: toothbrush, powered
Regulation Number: 872.6865
Classification Product Code: JEQ
Date Received: 03/02/1982
Decision Date: 04/27/1982
Regulation Medical Specialty: Dental
Device Name: ULTRASONIC TOOTHBRUSH
Manufacturer: ULTRASONIC PLAQUE CONTROL LABORATORIES
Device Classification Name: toothbrush, powered
Regulation Number: 872.6865
Classification Product Code: JEQ
Date Received: 03/02/1982
Decision Date: 04/27/1982
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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