FDA 510(k), K172545, SERI Contour

FDA 510(k), K172545, SERI Contour

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510(K) Number: K172545
Device Name: SERI Contour
Manufacturer: Anh Hoang
Device Classification Name: Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery
Regulation Number: OXF
Classification Product Code: 08/23/2017
Date Received: 09/22/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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