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FDA 510(k), K040858, ORALIEF THERAPY FOR SENSITIVE TEETH
FDA 510(k), K040858, ORALIEF THERAPY FOR SENSITIVE TEETH
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510(K) Number: K040858
Device Name: ORALIEF THERAPY FOR SENSITIVE TEETH
Manufacturer: DAVID C GREENSPAN
Device Classification Name: Varnish, Cavity
Regulation Number: LBH
Classification Product Code: 04/02/2004
Date Received: 09/02/2004
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: ORALIEF THERAPY FOR SENSITIVE TEETH
Manufacturer: DAVID C GREENSPAN
Device Classification Name: Varnish, Cavity
Regulation Number: LBH
Classification Product Code: 04/02/2004
Date Received: 09/02/2004
Decision Date: Substantially Equivalent (SESE)
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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