K-number	K936202
Device name	URINARY ALBUMIN TEST PACK
Applicant	Dupont Medical Products
Product code	JIQ
Device class	Class I
Decision date	May 9, 1994
Decision	Substantially Equivalent
Regulation	862.1645

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View the full FDA submission: accessdata.fda.gov

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URINARY ALBUMIN TEST PACK

Everything you need for a 510(k) submission. Nothing you don't.