FDA 510(k), K980298, FLOWABLE HYBRID
FDA 510(k), K980298, FLOWABLE HYBRID
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510(K) Number: K980298
Device Name: FLOWABLE HYBRID
Manufacturer: COSMEDENT, INC.
Device Classification Name: Coating, Filling Material, Resin
Regulation Number: 872.3310
Classification Product Code: EBD
Date Received: 01/27/1998
Decision Date: 03/09/1998
Regulation Medical Specialty: Dental
Device Name: FLOWABLE HYBRID
Manufacturer: COSMEDENT, INC.
Device Classification Name: Coating, Filling Material, Resin
Regulation Number: 872.3310
Classification Product Code: EBD
Date Received: 01/27/1998
Decision Date: 03/09/1998
Regulation Medical Specialty: Dental
- 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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