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FDA 510(k), K780003, ENDOSOLV E
FDA 510(k), K780003, ENDOSOLV E
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510(K) Number: K780003
Device Name: ENDOSOLV E
Manufacturer: SEPTODONT, INC.
Device Classification Name: cleanser, root canal
Regulation Number:
Classification Product Code: KJJ
Date Received: 12/29/1977
Decision Date: 01/20/1978
Regulation Medical Specialty:
Device Name: ENDOSOLV E
Manufacturer: SEPTODONT, INC.
Device Classification Name: cleanser, root canal
Regulation Number:
Classification Product Code: KJJ
Date Received: 12/29/1977
Decision Date: 01/20/1978
Regulation Medical Specialty:
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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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