K-number	K022755
Device name	LIFEGUARD
Applicant	Medtek, LLC
Product code	KHE
Device class	Class II
Decision date	Sep 24, 2002
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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LIFEGUARD

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