FDA 510(k)

MedHealth DVT compression Devices MHH900S/MHH900E

Número K: K231801 · 2023-12-14

Data da decisão2023-12-14

Código do produtoJOW

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

MedHealth DVT compression Devices MHH900S/MHH900E is the device name listed in this FDA 510(k) record. The listed applicant is Medhealth Medical Limited. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K231801. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MedHealth DVT compression Devices MHH900S/MHH900E?

MedHealth DVT compression Devices MHH900S/MHH900E is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Medhealth Medical Limited. The 510(k) number is K231801.

When did MedHealth DVT compression Devices MHH900S/MHH900E receive FDA 510(k) clearance?

MedHealth DVT compression Devices MHH900S/MHH900E received FDA 510(k) clearance on 2023-12-14, under 510(k) number K231801.

Who is the listed applicant for MedHealth DVT compression Devices MHH900S/MHH900E?

The FDA 510(k) record lists Medhealth Medical Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E?

The FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E is JOW.

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