K-number	K911749
Device name	L-LINEX-RAY FLUORESCENCE
Applicant	Montifore Medical Center
Product code	JAO
Device class	Class II
Decision date	Aug 20, 1991
Decision	Substantially Equivalent
Regulation	892.1220

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View the full FDA submission: accessdata.fda.gov

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L-LINEX-RAY FLUORESCENCE

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