STC Diagnostics Benzoylecgonine Eia

FDA 510(k) K915785 · Solarcare Technologies Corp,Inc.

Substantially Equivalent

510(k) numberK915785

Submission

Device name
STC Diagnostics Benzoylecgonine Eia
Applicant
Solarcare Technologies Corp,Inc.
Bethlehem, PA, US
Received
December 24, 1991
Decision date
March 11, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JXO – Enzyme Immunoassay, Cocaine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3250
Specialty
Clinical Toxicology

Other 510(k)s with product code JXO

510(k)DeviceApplicantDecision
K201228Psychemedics Homogeneous Enzyme Immunoassay for Cocaine in HairJXO · Traditional Psychemedics Corporation06/25/2021SE
K111925Psychemedics Cocaine EiaJXO · Traditional Psychemedics Corp.05/01/2012SE
K923314Automates Coma Plus Cocaine Metabolite AssayJXO · Traditional Serex, Inc.08/24/1992SE
K921140STC Diagnostics AUTO0LYTE Cocaine Metabolite EiaJXO · Traditional Solarcare Technologies Corp,Inc.08/20/1992SE
K913737Il Test(Tm) CocaineJXO · Traditional Instrumentation Laboratory CO12/03/1991SE

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Questions and answers

When was STC Diagnostics Benzoylecgonine Eia cleared by the FDA?

STC Diagnostics Benzoylecgonine Eia (K915785) received a 510(k) decision of Substantially Equivalent on March 11, 1992, 78 days after the submission was received.

What is the product code of K915785?

The FDA product code is JXO – Enzyme Immunoassay, Cocaine, a Class II (moderate risk) device regulated under 21 CFR 862.3250.