510(k) K202007

LZI Oxycodone III Enzyme Immunoassay by Lin-Zhi International, Inc. — Product Code DJG

K202007 is an FDA 510(k) premarket notification submitted by Lin-Zhi International, Inc. for the device "LZI Oxycodone III Enzyme Immunoassay". The FDA issued a decision of Substantially Equivalent on September 17, 2020. The device falls under product code DJG (Enzyme Immunoassay, Opiates), a Class II device regulated under 21 CFR 862.3650. Lin-Zhi International, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 17, 2020
Date Received
July 21, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Opiates
Device Class
Class II
Regulation Number
862.3650
Review Panel
TX
Submission Type