K-number	K023990
Device name	CHROMOCHECK PROTEIN C 25; CHROMOCHECK PROTEIN C 50
Applicant	Precision Biologic
Product code	GGP
Device class	Class II
Decision date	Mar 19, 2003
Decision	Substantially Equivalent
Regulation	864.7290

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View the full FDA submission: accessdata.fda.gov

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CHROMOCHECK PROTEIN C 25; CHROMOCHECK PROTEIN C 50

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