K-number	K150564
Device name	Spaulding Electrocardiograph 2100iQ
Applicant	Spaulding Clinical Research, LLC
Product code	DPS
Device class	Class II
Decision date	Aug 12, 2015
Decision	Substantially Equivalent
Regulation	870.2340

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Source

View the full FDA submission: accessdata.fda.gov

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Spaulding Electrocardiograph 2100iQ

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