K-number	K082056
Device name	ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
Applicant	Life-Tech, Inc.
Product code	FFX
Device class	Class II
Decision date	Nov 7, 2008
Decision	Substantially Equivalent
Regulation	876.1725

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View the full FDA submission: accessdata.fda.gov

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ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1

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