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FDA 510(k), K982616, IPS EMPRESS 2
FDA 510(k), K982616, IPS EMPRESS 2
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$149.00 USD
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510(K) Number: K982616
Device Name: IPS EMPRESS 2
Manufacturer: IVOCLAR NORTH AMERICA, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 07/27/1998
Decision Date: 09/08/1998
Regulation Medical Specialty: Dental
Device Name: IPS EMPRESS 2
Manufacturer: IVOCLAR NORTH AMERICA, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 07/27/1998
Decision Date: 09/08/1998
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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