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FDA 510(k), K962743, PULPDENT SODIUM HYPOCHLORITE SOLUTION
FDA 510(k), K962743, PULPDENT SODIUM HYPOCHLORITE SOLUTION
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510(K) Number: K962743
Device Name: PULPDENT SODIUM HYPOCHLORITE SOLUTION
Manufacturer: KENNETH J BERK
Device Classification Name: Cleanser, Root Canal
Regulation Number: KJJ
Classification Product Code: 07/15/1996
Date Received: 08/06/1996
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: PULPDENT SODIUM HYPOCHLORITE SOLUTION
Manufacturer: KENNETH J BERK
Device Classification Name: Cleanser, Root Canal
Regulation Number: KJJ
Classification Product Code: 07/15/1996
Date Received: 08/06/1996
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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