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FDA 510(k)

Vessel Closure Device (VCD177213P)

N.º K: K260677 · 2026-09-17

SolicitanteVcd Medical S.R.L.
Fecha de decisión2026-09-17
Código de productoFZP
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Vessel Closure Device (VCD177213P) is the device name listed in this FDA 510(k) record. The listed applicant is Vcd Medical S.R.L.. It received FDA 510(k) clearance on 2026-09-17 under 510(k) number K260677. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Vessel Closure Device (VCD177213P)?

Vessel Closure Device (VCD177213P) is a medical device that received FDA 510(k) clearance on 2026-09-17. The listed applicant is Vcd Medical S.R.L.. The 510(k) number is K260677.

When did Vessel Closure Device (VCD177213P) receive FDA 510(k) clearance?

Vessel Closure Device (VCD177213P) received FDA 510(k) clearance on 2026-09-17, under 510(k) number K260677.

Who is the listed applicant for Vessel Closure Device (VCD177213P)?

The FDA 510(k) record lists Vcd Medical S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vessel Closure Device (VCD177213P)?

The FDA product code for Vessel Closure Device (VCD177213P) is FZP.

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Fuente oficial

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