K-number	DEN160056
Device name	Philips IntelliSite Pathology Solution
Applicant	Philips Medical Systems Nederland B.V.
Product code	PSY
Device class	Class II
Decision date	Apr 12, 2017
Decision	Not Substantially Equivalent
Regulation	864.3700

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Source

View the full FDA submission: accessdata.fda.gov

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Philips IntelliSite Pathology Solution

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