K-number	K945556
Device name	ANTERIOR/POSTERIOR EPISTAXIS CATHETER
Applicant	Ultracell Medical Technologies, Inc.
Product code	EMX
Device class	Class I
Decision date	Jan 18, 1995
Decision	Substantially Equivalent
Regulation	874.4100

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View the full FDA submission: accessdata.fda.gov

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ANTERIOR/POSTERIOR EPISTAXIS CATHETER

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