K-number	K102900
Device name	HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM
Applicant	Hei, Inc.
Product code	LGZ
Device class	Class II
Decision date	Mar 21, 2012
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

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