K-number	K192259
Device name	Philips IntelliSite Pathology Solution
Applicant	Philips Electronics Nederland B.V.
Product code	PSY
Device class	Class II
Decision date	Sep 20, 2019
Decision	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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