510(k) K903824

DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY by Technicon Instruments Corp. — Product Code DKZ

K903824 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY". The FDA issued a decision of Substantially Equivalent on September 27, 1990. The device falls under product code DKZ (Enzyme Immunoassay, Amphetamine), a Class II device regulated under 21 CFR 862.3100. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1990
Date Received
August 20, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Amphetamine
Device Class
Class II
Regulation Number
862.3100
Review Panel
TX
Submission Type