K-number	K061396
Device name	QLAB QUANTIFICATION SOFTWARE
Applicant	Philips Ultrasound, Inc.
Product code	LLZ
Device class	Class II
Decision date	May 30, 2006
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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QLAB QUANTIFICATION SOFTWARE

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