510(k) K940123

METHAQUALONE ENZYME IMMUNOASSAY by Diagnostic Reagents, Inc. — Product Code KXS

K940123 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "METHAQUALONE ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on May 3, 1994. The device falls under product code KXS (Radioimmunoassay, Methaqualone), a Class II device regulated under 21 CFR 862.3630. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 3, 1994
Date Received
January 10, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Methaqualone
Device Class
Class II
Regulation Number
862.3630
Review Panel
TX
Submission Type