K-number	K221901
Device name	EleGARD
Applicant	Advancedcpr Solutions, LLC
Product code	FOA
Device class	Class I
Decision date	Jul 29, 2022
Decision	Substantially Equivalent
Regulation	880.6080

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Source

View the full FDA submission: accessdata.fda.gov

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EleGARD

Everything you need for a 510(k) submission. Nothing you don't.