510(k) K023109

AMEDICA DRUG SCREEN PHENCYCLIDINE TEST by Amedica Biotech, Inc. — Product Code LCM

K023109 is an FDA 510(k) premarket notification submitted by Amedica Biotech, Inc. for the device "AMEDICA DRUG SCREEN PHENCYCLIDINE TEST". The FDA issued a decision of Substantially Equivalent on December 16, 2002. The device falls under product code LCM (Enzyme Immunoassay, Phencyclidine), a Class U device. Amedica Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 16, 2002
Date Received
September 18, 2002
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