510(k) K961988

VALPROIC ACID EIA TEST by Diagnostic Reagents, Inc. — Product Code LEG

K961988 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "VALPROIC ACID EIA TEST". The FDA issued a decision of Substantially Equivalent on July 16, 1996. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 1996
Date Received
May 21, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Valproic Acid
Device Class
Class II
Regulation Number
862.3645
Review Panel
TX
Submission Type