K-number	K233662
Device name	Radiography 7300 C
Applicant	Philips Medical Systems Dmc GmbH
Product code	KPR
Device class	Class II
Decision date	Jun 13, 2024
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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Radiography 7300 C

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