FDA 510(k)

Patient Monitoring Cable (SpO2 Extension Cable)

N.º K: K192404 · 2020-06-22

SolicitanteShenzhen Coreray Technology, Ltd.

Fecha de decisión2020-06-22

Código de productoDSA

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Patient Monitoring Cable (SpO2 Extension Cable) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Coreray Technology, Ltd.. It received FDA 510(k) clearance on 2020-06-22 under 510(k) number K192404. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Patient Monitoring Cable (SpO2 Extension Cable)?

Patient Monitoring Cable (SpO2 Extension Cable) is a medical device that received FDA 510(k) clearance on 2020-06-22. The listed applicant is Shenzhen Coreray Technology, Ltd.. The 510(k) number is K192404.

When did Patient Monitoring Cable (SpO2 Extension Cable) receive FDA 510(k) clearance?

Patient Monitoring Cable (SpO2 Extension Cable) received FDA 510(k) clearance on 2020-06-22, under 510(k) number K192404.

Who is the listed applicant for Patient Monitoring Cable (SpO2 Extension Cable)?

The FDA 510(k) record lists Shenzhen Coreray Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Patient Monitoring Cable (SpO2 Extension Cable)?

The FDA product code for Patient Monitoring Cable (SpO2 Extension Cable) is DSA.

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Otros registros que enlistan a Shenzhen Coreray Technology, Ltd. como solicitante

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Dispositivos relacionados (Código: DSA)

Fuente oficial

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