K-number	K001397
Device name	QUICKSCREEN PRO DRUG CUP, MODEL 9195X
Applicant	Phamatech
Product code	DKZ
Device class	Class II
Decision date	May 26, 2000
Decision	Substantially Equivalent
Regulation	862.3100

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View the full FDA submission: accessdata.fda.gov

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QUICKSCREEN PRO DRUG CUP, MODEL 9195X

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