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FDA 510(k)

Vessel Closure Device (VCD177213P)

K-Number: K260677 · 2026-09-17

ApplicantVcd Medical S.R.L.
Decision Date2026-09-17
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Related Devices (Code: FZP)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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