K-number	K981966
Device name	NOSEBLEED NOSECLIP
Applicant	Michael M. Knott, M.D.
Product code	EMX
Device class	Class I
Decision date	Aug 14, 1998
Decision	Substantially Equivalent
Regulation	874.4100

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View the full FDA submission: accessdata.fda.gov

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NOSEBLEED NOSECLIP

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