FDA 510(k), K875145, MAR BOND

FDA 510(k), K875145, MAR BOND

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510(K) Number: K875145
Device Name: MAR BOND
Manufacturer: PAUL A GANGE
Device Classification Name: Crown And Bridge, Temporary, Resin
Regulation Number: EBG
Classification Product Code: KXA
Date Received: 12/15/1987
Decision Date: 02/26/1988
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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