K-number	K081565
Device name	INTEGRE PRO, MODEL L2RY
Applicant	Ellex Medical Pty, Ltd.
Product code	HQF
Device class	Class II
Decision date	Jul 2, 2008
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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INTEGRE PRO, MODEL L2RY

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