K-number	K890409
Device name	DADE(R) PLASMINOGEN CHROMOGENIC ASSAY
Applicant	Baxter Healthcare Corp
Product code	GGP
Device class	Class II
Decision date	Feb 27, 1989
Decision	Substantially Equivalent
Regulation	864.7290

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View the full FDA submission: accessdata.fda.gov

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DADE(R) PLASMINOGEN CHROMOGENIC ASSAY

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