K-number	K914381
Device name	HORIZON 9000/HIS OPTION AMPLIFIER
Applicant	Mennen Medical, Inc.
Product code	DRR
Device class	Class II
Decision date	Jan 28, 1992
Decision	Substantially Equivalent
Regulation	870.2050

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View the full FDA submission: accessdata.fda.gov

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HORIZON 9000/HIS OPTION AMPLIFIER

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