K-number	K021114
Device name	'RAPIDTEC' 5A MULTIPLE DIP TEST
Applicant	American Bio Medica Corp.
Product code	DKZ
Device class	Class II
Decision date	Jul 23, 2002
Decision	Substantially Equivalent
Regulation	862.3100

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View the full FDA submission: accessdata.fda.gov

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'RAPIDTEC' 5A MULTIPLE DIP TEST

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