K-number	K023785
Device name	LUNG NODULE ASSESSMENT AND COMPARISON OPTION
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	JAK
Device class	Class II
Decision date	Feb 10, 2003
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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LUNG NODULE ASSESSMENT AND COMPARISON OPTION

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