FDA 510(k)

MSC SFM

N.º K: K232543 · 2024-09-06

SolicitanteYocon Biology Technology Company

Fecha de decisión2024-09-06

Código de productoNDS

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

MSC SFM is the device name listed in this FDA 510(k) record. The listed applicant is Yocon Biology Technology Company. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K232543. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MSC SFM?

MSC SFM is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Yocon Biology Technology Company. The 510(k) number is K232543.

When did MSC SFM receive FDA 510(k) clearance?

MSC SFM received FDA 510(k) clearance on 2024-09-06, under 510(k) number K232543.

Who is the listed applicant for MSC SFM?

The FDA 510(k) record lists Yocon Biology Technology Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSC SFM?

The FDA product code for MSC SFM is NDS.

Dispositivos relacionados (Código: NDS)

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K240247“MoFi” Cell Culture Basal MediumDuogenic Stemcells Corporation K231804PRIME-XV FreezIS DMSO-Free MDFujifilm Irvine Scientific K201789CT-STOREnergy Delivery Solutions

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.