K-number	K111939
Device name	M/29TM - PRESSURE INJECTABLE
Applicant	Flexicath , Ltd.
Product code	FOZ
Device class	Class II
Decision date	Jul 11, 2012
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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M/29TM - PRESSURE INJECTABLE

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