Opus Carbamazepine Test System

FDA 510(k) K896860 · Pb Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK896860

Submission

Device name
Opus Carbamazepine Test System
Applicant
Pb Diagnostic Systems, Inc.
Westwood, MA, US
Received
December 5, 1989
Decision date
January 2, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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Questions and answers

When was Opus Carbamazepine Test System cleared by the FDA?

Opus Carbamazepine Test System (K896860) received a 510(k) decision of Substantially Equivalent on January 2, 1990, 28 days after the submission was received.

What is the product code of K896860?

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