K-number	K093546
Device name	SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX
Applicant	Togo Medikit Co., Ltd.
Product code	FOZ
Device class	Class II
Decision date	Dec 17, 2009
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX

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