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FDA 510(k), K143292, TheraCal DC
FDA 510(k), K143292, TheraCal DC
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510(K) Number: K143292
Device Name: TheraCal DC
Manufacturer: Bisco Inc
Device Classification Name: liner, cavity, calcium hydroxide
Regulation Number: 872.3250
Classification Product Code: EJK
Date Received: 11/17/2014
Decision Date: 08/04/2015
Regulation Medical Specialty: Dental
Device Name: TheraCal DC
Manufacturer: Bisco Inc
Device Classification Name: liner, cavity, calcium hydroxide
Regulation Number: 872.3250
Classification Product Code: EJK
Date Received: 11/17/2014
Decision Date: 08/04/2015
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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