FDA 510(k)

Bio-MEM Ti Reinforced Membrane

N.º K: K210797 · 2022-08-18

Fecha de decisión2022-08-18

Código de productoNPK

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Bio-MEM Ti Reinforced Membrane is the device name listed in this FDA 510(k) record. The listed applicant is B&Medi Co., Ltd.. It received FDA 510(k) clearance on 2022-08-18 under 510(k) number K210797. The device is classified under product code NPK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Bio-MEM Ti Reinforced Membrane?

Bio-MEM Ti Reinforced Membrane is a medical device that received FDA 510(k) clearance on 2022-08-18. The listed applicant is B&Medi Co., Ltd.. The 510(k) number is K210797.

When did Bio-MEM Ti Reinforced Membrane receive FDA 510(k) clearance?

Bio-MEM Ti Reinforced Membrane received FDA 510(k) clearance on 2022-08-18, under 510(k) number K210797.

Who is the listed applicant for Bio-MEM Ti Reinforced Membrane?

The FDA 510(k) record lists B&Medi Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bio-MEM Ti Reinforced Membrane?

The FDA product code for Bio-MEM Ti Reinforced Membrane is NPK.

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