FDA 510(k)

QUEX ED; QUEX S

Número K: K232779 · 2024-10-11

Data da decisão2024-10-11

Código do produtoOMC

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

QUEX ED; QUEX S is the device name listed in this FDA 510(k) record. The listed applicant is Qx World, Ltd.. It received FDA 510(k) clearance on 2024-10-11 under 510(k) number K232779. The device is classified under product code OMC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the QUEX ED; QUEX S?

QUEX ED; QUEX S is a medical device that received FDA 510(k) clearance on 2024-10-11. The listed applicant is Qx World, Ltd.. The 510(k) number is K232779.

When did QUEX ED; QUEX S receive FDA 510(k) clearance?

QUEX ED; QUEX S received FDA 510(k) clearance on 2024-10-11, under 510(k) number K232779.

Who is the listed applicant for QUEX ED; QUEX S?

The FDA 510(k) record lists Qx World, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUEX ED; QUEX S?

The FDA product code for QUEX ED; QUEX S is OMC.

Dispositivos Relacionados (Código: OMC)

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