FDA 510(k)

Spencer Probe Depth Electrodes

N.º K: K223269 · 2023-05-18

SolicitanteAd-Tech Medical Instrument Corporation

Fecha de decisión2023-05-18

Código de productoGZL

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Spencer Probe Depth Electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Ad-Tech Medical Instrument Corporation. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K223269. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Spencer Probe Depth Electrodes?

Spencer Probe Depth Electrodes is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Ad-Tech Medical Instrument Corporation. The 510(k) number is K223269.

When did Spencer Probe Depth Electrodes receive FDA 510(k) clearance?

Spencer Probe Depth Electrodes received FDA 510(k) clearance on 2023-05-18, under 510(k) number K223269.

Who is the listed applicant for Spencer Probe Depth Electrodes?

The FDA 510(k) record lists Ad-Tech Medical Instrument Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spencer Probe Depth Electrodes?

The FDA product code for Spencer Probe Depth Electrodes is GZL.

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Otros registros que enlistan a Ad-Tech Medical Instrument Corporation como solicitante

K223276Bujones Anchor como Accesorios de Electrodos de Profundidad K191186Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode K181544Anchor Bolt (como accesorio de Electrodos de Profundidad)K170442Cranial Drill Bits and Accessories K163355Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth Electrodes, Spencer Probe Depth Electrodes K152769FREMAP ELECTRODE

Ver todos los 8 dispositivos →

Dispositivos relacionados (Código: GZL)

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.