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FDA 510(k)

TIVA¿

K-Number: K152924 · 2016-01-07

Decision Date2016-01-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TIVA¿ is the device name listed in this FDA 510(k) record. The listed applicant is Velano Vascular. It received FDA 510(k) clearance on 2016-01-07 under 510(k) number K152924. 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 TIVA¿?

TIVA¿ is a medical device that received FDA 510(k) clearance on 2016-01-07. The listed applicant is Velano Vascular. The 510(k) number is K152924.

When did TIVA¿ receive FDA 510(k) clearance?

TIVA¿ received FDA 510(k) clearance on 2016-01-07, under 510(k) number K152924.

Who is the listed applicant for TIVA¿?

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

What is the FDA product code for TIVA¿?

The FDA product code for TIVA¿ is JKA.

Other records listing Velano Vascular as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: JKA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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