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FDA 510(k), K062653, MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098
FDA 510(k), K062653, MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098
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510(K) Number: K062653
Device Name: MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098
Manufacturer: PARNELL PHARMACEUTICALS, INC.
Device Classification Name: saliva, artificial
Regulation Number:
Classification Product Code: LFD
Date Received: 09/07/2006
Decision Date: 10/27/2006
Regulation Medical Specialty:
Device Name: MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098
Manufacturer: PARNELL PHARMACEUTICALS, INC.
Device Classification Name: saliva, artificial
Regulation Number:
Classification Product Code: LFD
Date Received: 09/07/2006
Decision Date: 10/27/2006
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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