K-number	K052557
Device name	SUPER SHEATH INTRODUCER SHEATH
Applicant	Togo Medikit Co., Ltd.
Product code	DRE
Device class	Class II
Decision date	Jan 17, 2006
Decision	Substantially Equivalent
Regulation	870.1310

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Source

View the full FDA submission: accessdata.fda.gov

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SUPER SHEATH INTRODUCER SHEATH

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