FDA 510(k), K083695, TRAXODENT
FDA 510(k), K083695, TRAXODENT
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510(K) Number: K083695
Device Name: TRAXODENT
Manufacturer: PREMIER DENTAL PRODUCTS CO.
Device Classification Name: cord, retraction
Regulation Number:
Classification Product Code: MVL
Date Received: 12/15/2008
Decision Date: 04/28/2009
Regulation Medical Specialty:
Device Name: TRAXODENT
Manufacturer: PREMIER DENTAL PRODUCTS CO.
Device Classification Name: cord, retraction
Regulation Number:
Classification Product Code: MVL
Date Received: 12/15/2008
Decision Date: 04/28/2009
Regulation Medical Specialty:
- 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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