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FDA 510(k)

Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford

N.º K: K163292 · 2017-09-08

SolicitanteSpectra Medical Devices
Fecha de decisión2017-09-08
Código de productoBSP
Comité asesorAN
DecisiónSubstantially Equivalent

Resumen del dispositivo

Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford is the device name listed in this FDA 510(k) record. The listed applicant is Spectra Medical Devices. It received FDA 510(k) clearance on 2017-09-08 under 510(k) number K163292. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford?

Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford is a medical device that received FDA 510(k) clearance on 2017-09-08. The listed applicant is Spectra Medical Devices. The 510(k) number is K163292.

When did Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford receive FDA 510(k) clearance?

Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford received FDA 510(k) clearance on 2017-09-08, under 510(k) number K163292.

Who is the listed applicant for Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford?

The FDA 510(k) record lists Spectra Medical Devices as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford?

The FDA product code for Sonic Block Tuohy, Sonic Block Quincke, Sonic Block Chiba, Sonic Block Crawford is BSP.

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Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

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

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