K-number	K902237
Device name	MEDICA IIF ANTI-SKIN ANTIBODY TEST KIT
Applicant	Medica Corp.
Product code	DBL
Device class	Class II
Decision date	Jul 9, 1990
Decision	Substantially Equivalent
Regulation	866.5660

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View the full FDA submission: accessdata.fda.gov

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MEDICA IIF ANTI-SKIN ANTIBODY TEST KIT

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