510(k) K972526

METHADONE EIA ASSAY by Diagnostic Reagents, Inc. — Product Code DJR

K972526 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "METHADONE EIA ASSAY". The FDA issued a decision of Substantially Equivalent on August 4, 1997. The device falls under product code DJR (Enzyme Immunoassay, Methadone), a Class II device regulated under 21 CFR 862.3620. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 4, 1997
Date Received
June 26, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Methadone
Device Class
Class II
Regulation Number
862.3620
Review Panel
TX
Submission Type