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FDA 510(k), K875142, PHASE II
FDA 510(k), K875142, PHASE II
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510(K) Number: K875142
Device Name: PHASE II
Manufacturer: PAUL A GANGE
Device Classification Name: Adhesive, Bracket And Tooth Conditioner, Resin
Regulation Number: DYH
Classification Product Code: 12/15/1987
Date Received: 02/29/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: PHASE II
Manufacturer: PAUL A GANGE
Device Classification Name: Adhesive, Bracket And Tooth Conditioner, Resin
Regulation Number: DYH
Classification Product Code: 12/15/1987
Date Received: 02/29/1988
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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