K-number	K141504
Device name	T-8000 THEROZONE UNIT
Applicant	Therozone USA, Inc.
Product code	EIA
Device class	Class I
Decision date	Feb 24, 2015
Decision	Substantially Equivalent
Regulation	872.6640

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View the full FDA submission: accessdata.fda.gov

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T-8000 THEROZONE UNIT

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