FDA 510(k)

PCA-C1 series Patient Cable

N.º K: K200722 · 2021-06-03

Fecha de decisión2021-06-03

Código de productoDSA

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

PCA-C1 series Patient Cable is the device name listed in this FDA 510(k) record. The listed applicant is QT Medical, Inc.. It received FDA 510(k) clearance on 2021-06-03 under 510(k) number K200722. 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 PCA-C1 series Patient Cable?

PCA-C1 series Patient Cable is a medical device that received FDA 510(k) clearance on 2021-06-03. The listed applicant is QT Medical, Inc.. The 510(k) number is K200722.

When did PCA-C1 series Patient Cable receive FDA 510(k) clearance?

PCA-C1 series Patient Cable received FDA 510(k) clearance on 2021-06-03, under 510(k) number K200722.

Who is the listed applicant for PCA-C1 series Patient Cable?

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

What is the FDA product code for PCA-C1 series Patient Cable?

The FDA product code for PCA-C1 series Patient Cable is DSA.

Ensayos clínicos relacionados

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Otros registros que enlistan a QT Medical, Inc. como solicitante

K233521QT ECG (QTERD100)K220795QT ECG K180157QT ECG

Dispositivos relacionados (Código: DSA)

Fuente oficial

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