K-number	K223311
Device name	Philips CT 3500
Applicant	Philips Healthcare (Suzhou) Co., Ltd.
Product code	JAK
Device class	Class II
Decision date	Dec 22, 2022
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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Philips CT 3500

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