K-number	K970539
Device name	CHIRON DIAGNOSTICS ACS:180TU P
Applicant	Chiron Diagnostics Corp.
Product code	KHQ
Device class	Class II
Decision date	Mar 24, 1997
Decision	Substantially Equivalent
Regulation	862.1715

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View the full FDA submission: accessdata.fda.gov

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CHIRON DIAGNOSTICS ACS:180TU P

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