K-number	K031505
Device name	RAPIDO CUT-AWAY GUIDING CATHETER
Applicant	Guidant Corporation
Product code	DQY
Device class	Class II
Decision date	Jun 25, 2003
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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RAPIDO CUT-AWAY GUIDING CATHETER

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