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FDA 510(k), K152490, DERMABOND PRINEO Skin Closure System
FDA 510(k), K152490, DERMABOND PRINEO Skin Closure System
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510(K) Number: K152490
Device Name: DERMABOND PRINEO Skin Closure System
Manufacturer: DONNA MARSHALL
Device Classification Name: Cutaneous Tissue Adhesive With Mesh
Regulation Number: OMD
Classification Product Code: 09/01/2015
Date Received: 11/25/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: DERMABOND PRINEO Skin Closure System
Manufacturer: DONNA MARSHALL
Device Classification Name: Cutaneous Tissue Adhesive With Mesh
Regulation Number: OMD
Classification Product Code: 09/01/2015
Date Received: 11/25/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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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