K-number	K233753
Device name	AI-Rad Companion (Pulmonary)
Applicant	Siemens Healthcare GmbH
Product code	JAK
Device class	Class II
Decision date	Mar 21, 2024
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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AI-Rad Companion (Pulmonary)

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