K-number	K233678
Device name	Radiography 7000 M
Applicant	Philips Medical Systems Dmc GmbH
Product code	IZL
Device class	Class II
Decision date	Feb 14, 2024
Decision	Substantially Equivalent
Regulation	892.1720

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Source

View the full FDA submission: accessdata.fda.gov

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Radiography 7000 M

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