K-number	K162484
Device name	Lung Nodule Assessment and Comparison Option (LNA)
Applicant	Philips Medical Systems Nederland B.V.
Product code	LLZ
Device class	Class II
Decision date	Feb 23, 2017
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Lung Nodule Assessment and Comparison Option (LNA)

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