510(k) K830461

ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE by Hoffmann-La Roche, Inc. — Product Code KXS

K830461 is an FDA 510(k) premarket notification submitted by Hoffmann-La Roche, Inc. for the device "ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE". The FDA issued a decision of Substantially Equivalent on March 24, 1983. The device falls under product code KXS (Radioimmunoassay, Methaqualone), a Class II device regulated under 21 CFR 862.3630. Hoffmann-La Roche, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 24, 1983
Date Received
February 15, 1983
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