510(k) K934061

BIOTRACK VALPROIC ACID TEST CARTRIDGE by Biotrack, Inc. — Product Code LEG

K934061 is an FDA 510(k) premarket notification submitted by Biotrack, Inc. for the device "BIOTRACK VALPROIC ACID TEST CARTRIDGE". The FDA issued a decision of Substantially Equivalent on December 29, 1993. The device falls under product code LEG (Enzyme Immunoassay, Valproic Acid), a Class II device regulated under 21 CFR 862.3645. Biotrack, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 29, 1993
Date Received
August 19, 1993
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