510(k) K002776

MODIFICATION TO PROFILE -II by Medtox Diagnostics, Inc. — Product Code LCM

K002776 is an FDA 510(k) premarket notification submitted by Medtox Diagnostics, Inc. for the device "MODIFICATION TO PROFILE -II". The FDA issued a decision of Substantially Equivalent on September 28, 2000. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Medtox Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 28, 2000
Date Received
September 6, 2000
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Phencyclidine
Device Class
Class U
Regulation Number
Review Panel
TX
Submission Type