K-number	K991252
Device name	AIA-PACK FT3 ASSAY
Applicant	Tosoh Medics, Inc.
Product code	CDP
Device class	Class II
Decision date	May 11, 1999
Decision	Substantially Equivalent
Regulation	862.1710

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View the full FDA submission: accessdata.fda.gov

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AIA-PACK FT3 ASSAY

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