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FDA 510(k), K130180, CLEANSER ROOT CANAL
FDA 510(k), K130180, CLEANSER ROOT CANAL
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510(K) Number: K130180
Device Name: CLEANSER ROOT CANAL
Manufacturer: CERKAMED WOJCIECH PAWLOWSKI
Device Classification Name: cleanser, root canal
Regulation Number:
Classification Product Code: KJJ
Date Received: 01/25/2013
Decision Date: 10/03/2013
Regulation Medical Specialty:
Device Name: CLEANSER ROOT CANAL
Manufacturer: CERKAMED WOJCIECH PAWLOWSKI
Device Classification Name: cleanser, root canal
Regulation Number:
Classification Product Code: KJJ
Date Received: 01/25/2013
Decision Date: 10/03/2013
Regulation Medical Specialty:
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- 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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