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FDA 510(k), K062961, MICROLUX TRANSILLUMINATOR
FDA 510(k), K062961, MICROLUX TRANSILLUMINATOR
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510(K) Number: K062961
Device Name: MICROLUX TRANSILLUMINATOR
Manufacturer: ADDENT, INC.
Device Classification Name: caries detector, laser light, transmission
Regulation Number: 872.1745
Classification Product Code: NTK
Date Received: 09/29/2006
Decision Date: 02/08/2007
Regulation Medical Specialty: Dental
Device Name: MICROLUX TRANSILLUMINATOR
Manufacturer: ADDENT, INC.
Device Classification Name: caries detector, laser light, transmission
Regulation Number: 872.1745
Classification Product Code: NTK
Date Received: 09/29/2006
Decision Date: 02/08/2007
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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