K-number	K911270
Device name	LEOCOR GUIDING CATHETER
Applicant	Leocor, Inc.
Product code	DQO
Device class	Class II
Decision date	Jan 17, 1992
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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LEOCOR GUIDING CATHETER

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