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FDA 510(k), K961199, BOSWORTH TEMPORARY RESIN
FDA 510(k), K961199, BOSWORTH TEMPORARY RESIN
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510(K) Number: K961199
Device Name: BOSWORTH TEMPORARY RESIN
Manufacturer: MILDRED M GOLDSTEIN
Device Classification Name: Crown And Bridge, Temporary, Resin
Regulation Number: EBG
Classification Product Code: 03/27/1996
Date Received: 06/25/1996
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: BOSWORTH TEMPORARY RESIN
Manufacturer: MILDRED M GOLDSTEIN
Device Classification Name: Crown And Bridge, Temporary, Resin
Regulation Number: EBG
Classification Product Code: 03/27/1996
Date Received: 06/25/1996
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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