FDA 510(k)

Negative Pressure Wound Therapy Device (V-Move, V-Grand)

Número K: K241023 · 2024-08-19

Data da decisão2024-08-19

Código do produtoOMP

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Negative Pressure Wound Therapy Device (V-Move, V-Grand) is the device name listed in this FDA 510(k) record. The listed applicant is Med Way, Inc.. It received FDA 510(k) clearance on 2024-08-19 under 510(k) number K241023. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

Negative Pressure Wound Therapy Device (V-Move, V-Grand) is a medical device that received FDA 510(k) clearance on 2024-08-19. The listed applicant is Med Way, Inc.. The 510(k) number is K241023.

When did Negative Pressure Wound Therapy Device (V-Move, V-Grand) receive FDA 510(k) clearance?

Negative Pressure Wound Therapy Device (V-Move, V-Grand) received FDA 510(k) clearance on 2024-08-19, under 510(k) number K241023.

Who is the listed applicant for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

The FDA 510(k) record lists Med Way, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand)?

The FDA product code for Negative Pressure Wound Therapy Device (V-Move, V-Grand) is OMP.

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