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FDA 510(k)

Vyvo

K-Number: K231288 · 2024-03-04

Decision Date2024-03-04
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Vyvo is the device name listed in this FDA 510(k) record. The listed applicant is Vyvo Technology Corp.(Vt). It received FDA 510(k) clearance on 2024-03-04 under 510(k) number K231288. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vyvo?

Vyvo is a medical device that received FDA 510(k) clearance on 2024-03-04. The listed applicant is Vyvo Technology Corp.(Vt). The 510(k) number is K231288.

When did Vyvo receive FDA 510(k) clearance?

Vyvo received FDA 510(k) clearance on 2024-03-04, under 510(k) number K231288.

Who is the listed applicant for Vyvo?

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

What is the FDA product code for Vyvo?

The FDA product code for Vyvo is DQA.

Related Devices (Code: DQA)

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.