FDA 510(k)

Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit

N.º K: K173732 · 2018-08-23

SolicitanteThe Binding Site Group , Ltd.

Fecha de decisión2018-08-23

Código de productoDFH

Comité asesorIM

DecisiónSubstantially Equivalent

Resumen del dispositivo

Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site Group , Ltd.. It received FDA 510(k) clearance on 2018-08-23 under 510(k) number K173732. The device is classified under product code DFH. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit?

Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit is a medical device that received FDA 510(k) clearance on 2018-08-23. The listed applicant is The Binding Site Group , Ltd.. The 510(k) number is K173732.

When did Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit receive FDA 510(k) clearance?

Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit received FDA 510(k) clearance on 2018-08-23, under 510(k) number K173732.

Who is the listed applicant for Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit?

The FDA 510(k) record lists The Binding Site Group , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit?

The FDA product code for Optilite Freelite Mx Kappa Free Kit, Optilite Freelite Mx Lambda Free Kit is DFH.

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Otros registros que enlistan a The Binding Site Group , Ltd. como solicitante

K250159Immunoglobulin Isotypes (GAM) for the EXENT Analyser; EXENT Analyser K250549Optilite® Freelite Mx Kappa Free Kit; Optilite® Freelite Mx Lambda Free Kit K192116Human IgA liquid reagent kit for Use on SPAPlus K191985Optilite IgA Kit K191635Optilite IgM Kit K191465Human IgM Kit for use on SPAPlus

Ver todos los 17 dispositivos →

Dispositivos relacionados (Código: DFH)

K253358Diazyme Human Kappa (k) Free Light Chain Assay; Diazyme Human Lambda (¿) Free Light Chain AssayDiazyme Laboratories, Inc.K250549Optilite® Freelite Mx Kappa Free Kit; Optilite® Freelite Mx Lambda Free KitThe Binding Site Group , Ltd.K231601FLC Kappa, FLC Lambda,FLC Control Level 1, FLC Control Level 2Sebia K231290Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free KitThe Binding Site, Ltd.K210623FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2Sebia K211648Diazyme Human Kappa Free Light Chain Assay, Diazyme Human Lambda Free Light Chain AssayDiazyme Laboratories, Inc.

Fuente oficial

Ver en la base de datos de la FDA →

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