K-number	K152311
Device name	Pentacam AXL
Applicant	Oculus Optikgerate GmbH
Product code	MXK
Device class	Class II
Decision date	Jan 20, 2016
Decision	Substantially Equivalent
Regulation	886.1850

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Source

View the full FDA submission: accessdata.fda.gov

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Pentacam AXL

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