K-number	K203428
Device name	Ziehm Vision RFD
Applicant	Ziehm Imaging GmbH
Product code	JAA
Device class	Class II
Decision date	Mar 17, 2021
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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Ziehm Vision RFD

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