K-number	K991074
Device name	BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST
Applicant	Intracel Corp.
Product code	MJH
Device class	Class II
Decision date	Dec 21, 1999
Decision	Substantially Equivalent
Regulation	866.3300

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View the full FDA submission: accessdata.fda.gov

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BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST

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