K-number	K910617
Device name	NATIVE PROTHROMBIN ANTIGEN EIA
Applicant	Organon Teknika Corp.
Product code	DDF
Device class	Class I
Decision date	May 15, 1991
Decision	Substantially Equivalent
Regulation	866.5735

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View the full FDA submission: accessdata.fda.gov

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NATIVE PROTHROMBIN ANTIGEN EIA

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