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FDA 510(k)

LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream

N.º K: K153719 · 2016-06-03

SolicitanteHoneywell Hommed, LLC
Fecha de decisión2016-06-03
Código de productoDRG
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell Hommed, LLC. It received FDA 510(k) clearance on 2016-06-03 under 510(k) number K153719. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?

LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream is a medical device that received FDA 510(k) clearance on 2016-06-03. The listed applicant is Honeywell Hommed, LLC. The 510(k) number is K153719.

When did LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream receive FDA 510(k) clearance?

LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream received FDA 510(k) clearance on 2016-06-03, under 510(k) number K153719.

Who is the listed applicant for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?

The FDA 510(k) record lists Honeywell Hommed, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream?

The FDA product code for LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream is DRG.

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Dispositivos relacionados (Código: DRG)

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Fuente oficial

Ver en la base de datos de la FDA →

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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