K-number	K111542
Device name	DELTEX MEDICAL CARDIOQ EDM
Applicant	Deltex Medical Limited
Product code	DPW
Device class	Class II
Decision date	Oct 20, 2011
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

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