510(k) K010138

PROFILE II ER by Medtox Diagnostics, Inc. — Product Code LDJ

K010138 is an FDA 510(k) premarket notification submitted by Medtox Diagnostics, Inc. for the device "PROFILE II ER". The FDA issued a decision of Substantially Equivalent on February 14, 2001. The device falls under product code LDJ (Enzyme Immunoassay, Cannabinoids), a Class II device regulated under 21 CFR 862.3870. Medtox Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 14, 2001
Date Received
January 17, 2001
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Cannabinoids
Device Class
Class II
Regulation Number
862.3870
Review Panel
TX
Submission Type