K-number	K080247
Device name	QUIKCLOT NOSEBLEED
Applicant	Z-Medica Corporation
Product code	LYA
Device class	Class I
Decision date	Feb 27, 2008
Decision	Substantially Equivalent
Regulation	874.4780

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View the full FDA submission: accessdata.fda.gov

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QUIKCLOT NOSEBLEED

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