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FDA 510(k), K123402, DIAGNOCAM
FDA 510(k), K123402, DIAGNOCAM
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510(K) Number: K123402
Device Name: DIAGNOCAM
Manufacturer: KALTENBACH & VOIGT GMBH
Device Classification Name: Caries Detector, Laser Light, Transmission
Regulation Number: 872.1745
Classification Product Code: NTK
Date Received: 11/05/2012
Decision Date: 09/24/2013
Regulation Medical Specialty: Dental
Device Name: DIAGNOCAM
Manufacturer: KALTENBACH & VOIGT GMBH
Device Classification Name: Caries Detector, Laser Light, Transmission
Regulation Number: 872.1745
Classification Product Code: NTK
Date Received: 11/05/2012
Decision Date: 09/24/2013
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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