K-number	K932084
Device name	AIA-PACK E2 ASSAY
Applicant	Tosoh Medics, Inc.
Product code	CHP
Device class	Class I
Decision date	Nov 9, 1993
Decision	Substantially Equivalent
Regulation	862.1260

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View the full FDA submission: accessdata.fda.gov

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AIA-PACK E2 ASSAY

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