K-number	K033436
Device name	REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
Applicant	Alliance Medical Corp.
Product code	OWQ
Device class	Class II
Decision date	Mar 16, 2005
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER

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