FDA 510(k)

SISTEMA DE MONITOREO DE ICP AURA

N.º K: K172209 · 2018-05-18

SolicitanteBranchpoint Technologies, Inc.

Fecha de decisión2018-05-18

Código de productoGWM

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

AURA ICP MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Branchpoint Technologies, Inc.. It received FDA 510(k) clearance on 2018-05-18 under 510(k) number K172209. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the AURA ICP MONITORING SYSTEM?

AURA ICP MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is Branchpoint Technologies, Inc.. The 510(k) number is K172209.

When did AURA ICP MONITORING SYSTEM receive FDA 510(k) clearance?

AURA ICP MONITORING SYSTEM received FDA 510(k) clearance on 2018-05-18, under 510(k) number K172209.

Who is the listed applicant for AURA ICP MONITORING SYSTEM?

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

What is the FDA product code for AURA ICP MONITORING SYSTEM?

The FDA product code for AURA ICP MONITORING SYSTEM is GWM.

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Fuente oficial

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