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FDA 510(k)

Velano Vascular Blood Collection Adapter

K-Number: K201237 · 2022-10-03

ApplicantVelano Vascular
Decision Date2022-10-03
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Velano Vascular Blood Collection Adapter is a medical device manufactured by Velano Vascular. It received FDA 510(k) clearance on 2022-10-03 under approval number K201237. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Velano Vascular Blood Collection Adapter?

Velano Vascular Blood Collection Adapter is a medical device that received FDA 510(k) clearance on 2022-10-03. It is manufactured by Velano Vascular. The 510(k) number is K201237.

When was Velano Vascular Blood Collection Adapter approved by the FDA?

Velano Vascular Blood Collection Adapter received FDA 510(k) clearance on 2022-10-03, under approval number K201237.

What company makes Velano Vascular Blood Collection Adapter?

Velano Vascular Blood Collection Adapter is manufactured by Velano Vascular.

What is the FDA product code for Velano Vascular Blood Collection Adapter?

The FDA product code for Velano Vascular Blood Collection Adapter is JKA.

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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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