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FDA 510(k), K112666, SALINE WOUND WASH
FDA 510(k), K112666, SALINE WOUND WASH
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510(K) Number: K112666
Device Name: SALINE WOUND WASH
Manufacturer: NANOPLAS, INC.
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 09/13/2011
Decision Date: 04/20/2012
Regulation Medical Specialty:
Device Name: SALINE WOUND WASH
Manufacturer: NANOPLAS, INC.
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 09/13/2011
Decision Date: 04/20/2012
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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