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FDA 510(k), K130852, AVANCE® FOAM ABDOMINAL DRESSING KIT
FDA 510(k), K130852, AVANCE® FOAM ABDOMINAL DRESSING KIT
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510(K) Number: K130852
Device Name: AVANCE® FOAM ABDOMINAL DRESSING KIT
Manufacturer: MOLNLYCKE HEALTHCARE
Device Classification Name: mesh, surgical, non-absorbable, large abdominal wall defects
Regulation Number: 878.3300
Classification Product Code: OXJ
Date Received: 03/28/2013
Decision Date: 04/14/2014
Regulation Medical Specialty: General & Plastic Surgery
Device Name: AVANCE® FOAM ABDOMINAL DRESSING KIT
Manufacturer: MOLNLYCKE HEALTHCARE
Device Classification Name: mesh, surgical, non-absorbable, large abdominal wall defects
Regulation Number: 878.3300
Classification Product Code: OXJ
Date Received: 03/28/2013
Decision Date: 04/14/2014
Regulation Medical Specialty: General & Plastic Surgery
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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. Learn more about Fast-Track Requests here.
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