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FDA 510(k)

IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit

N.º K: K210528 · 2022-03-16

SolicitanteMillennium Medical Technologies Inc (Dba Cellmyx)
Fecha de decisión2022-03-16
Código de productoMUU
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit is the device name listed in this FDA 510(k) record. The listed applicant is Millennium Medical Technologies Inc (Dba Cellmyx). It received FDA 510(k) clearance on 2022-03-16 under 510(k) number K210528. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit?

IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit is a medical device that received FDA 510(k) clearance on 2022-03-16. The listed applicant is Millennium Medical Technologies Inc (Dba Cellmyx). The 510(k) number is K210528.

When did IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit receive FDA 510(k) clearance?

IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit received FDA 510(k) clearance on 2022-03-16, under 510(k) number K210528.

Who is the listed applicant for IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit?

The FDA 510(k) record lists Millennium Medical Technologies Inc (Dba Cellmyx) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit?

The FDA product code for IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit is MUU.

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Dispositivos relacionados (Código: MUU)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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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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