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FDA 510(k), K110715, INTERDRY SILVER
FDA 510(k), K110715, INTERDRY SILVER
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510(K) Number: K110715
Device Name: INTERDRY SILVER
Manufacturer: MILLIKEN HEALTHCARE PRODUCTS, LLC
Device Classification Name: fiber, medical, absorbent
Regulation Number: 880.5300
Classification Product Code: FRL
Date Received: 03/15/2011
Decision Date: 11/04/2011
Regulation Medical Specialty: General Hospital
Device Name: INTERDRY SILVER
Manufacturer: MILLIKEN HEALTHCARE PRODUCTS, LLC
Device Classification Name: fiber, medical, absorbent
Regulation Number: 880.5300
Classification Product Code: FRL
Date Received: 03/15/2011
Decision Date: 11/04/2011
Regulation Medical Specialty: General Hospital
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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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