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FDA 510(k), K131487, FLUOR PROTECTOR S
FDA 510(k), K131487, FLUOR PROTECTOR S
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510(K) Number: K131487
Device Name: FLUOR PROTECTOR S
Manufacturer: IVOCLAR VIVADENT AG
Device Classification Name: Varnish, Cavity
Regulation Number: 872.3260
Classification Product Code: LBH
Date Received: 05/23/2013
Decision Date: 10/08/2014
Regulation Medical Specialty: Dental
Device Name: FLUOR PROTECTOR S
Manufacturer: IVOCLAR VIVADENT AG
Device Classification Name: Varnish, Cavity
Regulation Number: 872.3260
Classification Product Code: LBH
Date Received: 05/23/2013
Decision Date: 10/08/2014
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
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