K-number	K941192
Device name	ORTHO ALT MICROWELL TEST SYSTEM
Applicant	Ortho Diagnostic Systems, Inc.
Product code	CKD
Device class	Class I
Decision date	May 16, 1995
Decision	Substantially Equivalent
Regulation	862.1030

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View the full FDA submission: accessdata.fda.gov

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ORTHO ALT MICROWELL TEST SYSTEM

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