K-number	K210404
Device name	Transpara 1.7.0
Applicant	Screenpoint Medical B.V.
Product code	QDQ
Device class	Class II
Decision date	Jun 2, 2021
Decision	Substantially Equivalent
Regulation	892.2090

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Source

View the full FDA submission: accessdata.fda.gov

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Transpara 1.7.0

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