K-number	K790838
Device name	ARTERIAL EMBOLECTOMY CATHETER (MODIFIED)
Applicant	Shiley, Inc.
Product code	DXE
Device class	Class II
Decision date	Jun 11, 1979
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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ARTERIAL EMBOLECTOMY CATHETER (MODIFIED)

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