K-number	K090214
Device name	VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND
Applicant	Verathon Incorporated
Product code	IYO
Device class	Class II
Decision date	Mar 13, 2009
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND

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