FDA 510(k)

COBRA-OS Kit

N.º K: K201652 · 2021-02-22

SolicitanteFront Line Medical Technologies, Inc.

Fecha de decisión2021-02-22

Código de productoMJN

Comité asesorCV

DecisiónUnknown

Resumen del dispositivo

COBRA-OS Kit is the device name listed in this FDA 510(k) record. The listed applicant is Front Line Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-02-22 under 510(k) number K201652. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Preguntas frecuentes

What is the COBRA-OS Kit?

COBRA-OS Kit is a medical device that received FDA 510(k) clearance on 2021-02-22. The listed applicant is Front Line Medical Technologies, Inc.. The 510(k) number is K201652.

When did COBRA-OS Kit receive FDA 510(k) clearance?

COBRA-OS Kit received FDA 510(k) clearance on 2021-02-22, under 510(k) number K201652.

Who is the listed applicant for COBRA-OS Kit?

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

What is the FDA product code for COBRA-OS Kit?

The FDA product code for COBRA-OS Kit is MJN.

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Fuente oficial

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