K-number	K202094
Device name	Cardiovascular Suite 4.2.1
Applicant	Quipu S.R.L
Product code	DQK
Device class	Class II
Decision date	Jan 11, 2022
Decision	Substantially Equivalent
Regulation	870.1425

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Source

View the full FDA submission: accessdata.fda.gov

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Cardiovascular Suite 4.2.1

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