K-number	K993165
Device name	QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178
Applicant	Phamatech
Product code	DJG
Device class	Class II
Decision date	Oct 20, 1999
Decision	Substantially Equivalent
Regulation	862.3650

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View the full FDA submission: accessdata.fda.gov

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QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178

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