K-number	K791896
Device name	CENTRIA PHENYTOIN RIA TEST SET
Applicant	Ventrex Laboratories, Inc.
Product code	DLP
Device class	Class II
Decision date	Oct 17, 1979
Decision	Substantially Equivalent
Regulation	862.3350

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View the full FDA submission: accessdata.fda.gov

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CENTRIA PHENYTOIN RIA TEST SET

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