FDA 510(k), K031759, ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD AND ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD

FDA 510(k), K031759, ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD AND ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD

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510(K) Number: K031759
Device Name: ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD AND ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD
Manufacturer:
Device Classification Name: Enzyme Immunoassay, Amphetamine
Regulation Number: 862.3100
Classification Product Code: DKZ
Date Received: 06/06/2003
Decision Date: 08/04/2003
Regulation Medical Specialty: Toxicology
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