K-number	K172457
Device name	Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
Applicant	Deltex Medical Limited
Product code	DPW
Device class	Class II
Decision date	Jun 28, 2018
Decision	Substantially Equivalent
Regulation	870.2100

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Source

View the full FDA submission: accessdata.fda.gov

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Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM

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