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FDA 510(k), K896130, SR-IVOCAP
FDA 510(k), K896130, SR-IVOCAP
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510(K) Number: K896130
Device Name: SR-IVOCAP
Manufacturer: L SEVERANCE,DDS
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 10/23/1989
Date Received: 04/16/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: SR-IVOCAP
Manufacturer: L SEVERANCE,DDS
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 10/23/1989
Date Received: 04/16/1990
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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