K-number	K101406
Device name	ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001
Applicant	Medrad Interventional/Possis
Product code	QEZ
Device class	Class II
Decision date	Jun 16, 2010
Decision	Substantially Equivalent
Regulation	870.5150

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View the full FDA submission: accessdata.fda.gov

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ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

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