K-number	K130843
Device name	SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE
Applicant	Oscor, Inc.
Product code	DRC
Device class	Class II
Decision date	Jan 8, 2014
Decision	Substantially Equivalent
Regulation	870.1390

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Source

View the full FDA submission: accessdata.fda.gov

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SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE

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