510(k) K955100

CARBAMAZEPINE EIA TEST by Diagnostic Reagents, Inc. — Product Code KLT

K955100 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "CARBAMAZEPINE EIA TEST". The FDA issued a decision of Substantially Equivalent on December 13, 1995. The device falls under product code KLT (Enzyme Immunoassay, Carbamazepine), 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
December 13, 1995
Date Received
November 8, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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