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FDA 510(k)

Compremium Compartment Compressibility Monitoring System (CPM#1)

N.º K: K223509 · 2023-04-14

SolicitanteCompremium AG
Fecha de decisión2023-04-14
Código de productoLXC
DecisiónSubstantially Equivalent

Resumen del dispositivo

Compremium Compartment Compressibility Monitoring System (CPM#1) is the device name listed in this FDA 510(k) record. The listed applicant is Compremium AG. It received FDA 510(k) clearance on 2023-04-14 under 510(k) number K223509. The device is classified under product code LXC. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Compremium Compartment Compressibility Monitoring System (CPM#1)?

Compremium Compartment Compressibility Monitoring System (CPM#1) is a medical device that received FDA 510(k) clearance on 2023-04-14. The listed applicant is Compremium AG. The 510(k) number is K223509.

When did Compremium Compartment Compressibility Monitoring System (CPM#1) receive FDA 510(k) clearance?

Compremium Compartment Compressibility Monitoring System (CPM#1) received FDA 510(k) clearance on 2023-04-14, under 510(k) number K223509.

Who is the listed applicant for Compremium Compartment Compressibility Monitoring System (CPM#1)?

The FDA 510(k) record lists Compremium AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Compremium Compartment Compressibility Monitoring System (CPM#1)?

The FDA product code for Compremium Compartment Compressibility Monitoring System (CPM#1) is LXC.

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Fuente oficial

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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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