K-number	K003130
Device name	REGUTHERM 952 THERMOGRAPHIC SYSTEM
Applicant	Sie-Med, Inc.
Product code	LHQ
Device class	Class I
Decision date	Feb 16, 2001
Decision	Substantially Equivalent
Regulation	884.2980

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View the full FDA submission: accessdata.fda.gov

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REGUTHERM 952 THERMOGRAPHIC SYSTEM

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