K-number	K023869
Device name	'RAPIDTEC'-5M-MULTIPLE DIP TEST
Applicant	American Bio Medica Corp.
Product code	DJR
Device class	Class II
Decision date	Apr 30, 2003
Decision	Substantially Equivalent
Regulation	862.3620

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View the full FDA submission: accessdata.fda.gov

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'RAPIDTEC'-5M-MULTIPLE DIP TEST

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