K-number	K203845
Device name	Philips IntelliSite Pathology Solution
Applicant	Philips Medical Systems Nederland B.V.
Product code	PSY
Device class	Class II
Decision date	Sep 17, 2021
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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