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FDA 510(k), K093642, NEUTRASAL
FDA 510(k), K093642, NEUTRASAL
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510(K) Number: K093642
Device Name: NEUTRASAL
Manufacturer: INVADO PHARMACEUTICALS
Device Classification Name: saliva, artificial
Regulation Number:
Classification Product Code: LFD
Date Received: 11/24/2009
Decision Date: 12/11/2009
Regulation Medical Specialty:
Device Name: NEUTRASAL
Manufacturer: INVADO PHARMACEUTICALS
Device Classification Name: saliva, artificial
Regulation Number:
Classification Product Code: LFD
Date Received: 11/24/2009
Decision Date: 12/11/2009
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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