K-number	K915700
Device name	PERMIER HISTOPLASMA
Applicant	Meridian Diagnostics, Inc.
Product code	MIZ
Device class	Class II
Decision date	Jul 30, 1992
Decision	Substantially Equivalent
Regulation	866.3320

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View the full FDA submission: accessdata.fda.gov

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PERMIER HISTOPLASMA

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