K-number	K895160
Device name	ORTHO *APO A-1 ELISA TEST SYSTEM
Applicant	Medical Marketing Consultants, Inc.
Product code	DEL
Device class	Class I
Decision date	Oct 6, 1989
Decision	Substantially Equivalent
Regulation	866.5590

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View the full FDA submission: accessdata.fda.gov

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ORTHO *APO A-1 ELISA TEST SYSTEM

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