K-number	K041712
Device name	'RAPIDTEC 4' TEST
Applicant	American Bio Medica Corp.
Product code	DIS
Device class	Class II
Decision date	Nov 3, 2004
Decision	Substantially Equivalent
Regulation	862.3150

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Source

View the full FDA submission: accessdata.fda.gov

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'RAPIDTEC 4' TEST

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