K-number	K233945
Device name	ProxiDiagnost N90 / Precision CRF (706110, 706400)
Applicant	Philips Medical Systems Dmc GmbH
Product code	JAA
Device class	Class II
Decision date	Jan 11, 2024
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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ProxiDiagnost N90 / Precision CRF (706110, 706400)

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