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FDA 510(k), K864707, SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
FDA 510(k), K864707, SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
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510(K) Number: K864707
Device Name: SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
Manufacturer: BAUER, PHD
Device Classification Name: Denture, Plastic, Teeth
Regulation Number: ELM
Classification Product Code: 12/02/1986
Date Received: 02/10/1987
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH
Manufacturer: BAUER, PHD
Device Classification Name: Denture, Plastic, Teeth
Regulation Number: ELM
Classification Product Code: 12/02/1986
Date Received: 02/10/1987
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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