K-number	K892410
Device name	FOGARTY(R) THRU-LUMEN EMBOLECTOMY CATHETER
Applicant	Baxter Healthcare Corp
Product code	DXE
Device class	Class II
Decision date	Jul 20, 1989
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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FOGARTY(R) THRU-LUMEN EMBOLECTOMY CATHETER

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