K-number	K934550
Device name	IMMUNOCARD MYCOPLASMA
Applicant	Meridian Diagnostics, Inc.
Product code	LJZ
Device class	Class I
Decision date	Sep 20, 1994
Decision	Substantially Equivalent
Regulation	866.3375

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View the full FDA submission: accessdata.fda.gov

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IMMUNOCARD MYCOPLASMA

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