510(k) K874199

REVISED LABELING FOR SYVA METHAQUALONE ASSAYS by Syva Co. — Product Code KXS

K874199 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "REVISED LABELING FOR SYVA METHAQUALONE ASSAYS". The FDA issued a decision of Substantially Equivalent on October 28, 1987. The device falls under product code KXS (Radioimmunoassay, Methaqualone), a Class II device regulated under 21 CFR 862.3630. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 28, 1987
Date Received
October 14, 1987
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