510(k) K042807

ADVIA IMS VALPROIC ACID METHOD by Bayer Healthcare, LLC — Product Code LEG

K042807 is an FDA 510(k) premarket notification submitted by Bayer Healthcare, LLC for the device "ADVIA IMS VALPROIC ACID METHOD". The FDA issued a decision of Substantially Equivalent on February 8, 2005. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Bayer Healthcare, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 8, 2005
Date Received
October 12, 2004
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