K-number	K182790
Device name	Cardio-TriTest v6.5
Applicant	Cardio-Phoenix, Inc.
Product code	DPS
Device class	Class II
Decision date	Dec 14, 2018
Decision	Substantially Equivalent
Regulation	870.2340

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Source

View the full FDA submission: accessdata.fda.gov

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Cardio-TriTest v6.5

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