FDA 510(k)

MV Flow Aspiration Pump (MVFLOWPMP01)

Número K: K243638 · 2025-06-13

Data da decisão2025-06-13

Código do produtoJCX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

MV Flow Aspiration Pump (MVFLOWPMP01) is the device name listed in this FDA 510(k) record. The listed applicant is Microvention. It received FDA 510(k) clearance on 2025-06-13 under 510(k) number K243638. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MV Flow Aspiration Pump (MVFLOWPMP01)?

MV Flow Aspiration Pump (MVFLOWPMP01) is a medical device that received FDA 510(k) clearance on 2025-06-13. The listed applicant is Microvention. The 510(k) number is K243638.

When did MV Flow Aspiration Pump (MVFLOWPMP01) receive FDA 510(k) clearance?

MV Flow Aspiration Pump (MVFLOWPMP01) received FDA 510(k) clearance on 2025-06-13, under 510(k) number K243638.

Who is the listed applicant for MV Flow Aspiration Pump (MVFLOWPMP01)?

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

What is the FDA product code for MV Flow Aspiration Pump (MVFLOWPMP01)?

The FDA product code for MV Flow Aspiration Pump (MVFLOWPMP01) is JCX.

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