K-number	K951187
Device name	VARELISA CARDIOLIPIN ABS SCREEN
Applicant	Elias U.S.A., Inc.
Product code	MID
Device class	Class II
Decision date	Oct 2, 1995
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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VARELISA CARDIOLIPIN ABS SCREEN

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