510(k) K012582

AMEDITECH IMMUTEST DRUG SCREEN PCP by Ameditech, Inc. — Product Code LCM

K012582 is an FDA 510(k) premarket notification submitted by Ameditech, Inc. for the device "AMEDITECH IMMUTEST DRUG SCREEN PCP". The FDA issued a decision of Substantially Equivalent on November 30, 2001. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Ameditech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 2001
Date Received
August 10, 2001
Clearance Type
Traditional
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