K-number	K183322
Device name	physIQ Heart Rhythm and Respiratory Module
Applicant	Physiq, Inc.
Product code	DPS
Device class	Class II
Decision date	Jul 10, 2019
Decision	Substantially Equivalent
Regulation	870.2340

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Source

View the full FDA submission: accessdata.fda.gov

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physIQ Heart Rhythm and Respiratory Module

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