510(k) K982880

DIMENSION(R) VALPROIC (VALP) ACID METHOD by Dade Behring, Inc. — Product Code LEG

K982880 is an FDA 510(k) premarket notification submitted by Dade Behring, Inc. for the device "DIMENSION(R) VALPROIC (VALP) ACID METHOD". The FDA issued a decision of Substantially Equivalent on August 25, 1998. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Dade Behring, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 25, 1998
Date Received
August 14, 1998
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