K-number	K952412
Device name	DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL
Applicant	Dupont Medical Products
Product code	DIF
Device class	Class I
Decision date	Jun 23, 1995
Decision	Substantially Equivalent
Regulation	862.3280

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Source

View the full FDA submission: accessdata.fda.gov

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DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL

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