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FDA 510(k), K143001, SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
FDA 510(k), K143001, SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
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510(K) Number: K143001
Device Name: SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
Manufacturer: ARGENTUM MEDICAL
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/17/2014
Decision Date: 11/07/2014
Regulation Medical Specialty:
Device Name: SILVERLON ISLAND WOUND DRESSING, SILVERLON WOUND PAD DRESSING
Manufacturer: ARGENTUM MEDICAL
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 10/17/2014
Decision Date: 11/07/2014
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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