FDA 510(k), K152311, Pentacam AXL

FDA 510(k), K152311, Pentacam AXL

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510(K) Number: K152311
Device Name: Pentacam AXL
Manufacturer:
Device Classification Name: Device, Analysis, Anterior Segment
Regulation Number: 886.1850
Classification Product Code: MXK
Date Received: 08/14/2015
Decision Date: 01/20/2016
Regulation Medical Specialty: Ophthalmic
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