Carbamazepine Gen 4

FDA 510(k) K151578 · Roche Diagnostics Operations (Rdo)

Substantially Equivalent

510(k) numberK151578

Submission

Device name
Carbamazepine Gen 4
Applicant
Roche Diagnostics Operations (Rdo)
Indianapolis, IN, US
Received
June 11, 2015
Decision date
October 22, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KLT – Enzyme Immunoassay, Carbamazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3645
Specialty
Clinical Toxicology

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K063131Carbamazepine, Valproic Acid, TDM Calibration Set B and Abtrol, Nortrol ControlsKLT · Traditional Thermo Electron OY10/05/2007SE
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K011648Randox CarbamazepineKLT · Traditional Randox Laboratories, Ltd.01/15/2002SE
K010814Emit 2000 Carbamazepine Assay, Model OSR4F229KLT · Special Syva Co., Dade Behring, Inc.04/13/2001SE
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Questions and answers

When was Carbamazepine Gen 4 cleared by the FDA?

Carbamazepine Gen 4 (K151578) received a 510(k) decision of Substantially Equivalent on October 22, 2015, 133 days after the submission was received.

What is the product code of K151578?

The FDA product code is KLT – Enzyme Immunoassay, Carbamazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3645.