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FDA 510(k), K961735, ACTA
FDA 510(k), K961735, ACTA
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510(K) Number: K961735
Device Name: ACTA
Manufacturer: SATELEC
Device Classification Name: activator, ultraviolet, for polymerization
Regulation Number: 872.6070
Classification Product Code: EBZ
Date Received: 05/03/1996
Decision Date: 07/31/1996
Regulation Medical Specialty: Dental
Device Name: ACTA
Manufacturer: SATELEC
Device Classification Name: activator, ultraviolet, for polymerization
Regulation Number: 872.6070
Classification Product Code: EBZ
Date Received: 05/03/1996
Decision Date: 07/31/1996
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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