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FDA 510(k)

Accuro XV

K-Number: K254021 · 2026-04-09

ApplicantRivanna Medical, Inc.
Decision Date2026-04-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Accuro XV is a medical device manufactured by Rivanna Medical, Inc.. It received FDA 510(k) clearance on 2026-04-09 under approval number K254021. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Accuro XV?

Accuro XV is a medical device that received FDA 510(k) clearance on 2026-04-09. It is manufactured by Rivanna Medical, Inc.. The 510(k) number is K254021.

When was Accuro XV approved by the FDA?

Accuro XV received FDA 510(k) clearance on 2026-04-09, under approval number K254021.

What company makes Accuro XV?

Accuro XV is manufactured by Rivanna Medical, Inc..

What is the FDA product code for Accuro XV?

The FDA product code for Accuro XV is IYO.

Other Devices by Rivanna Medical, Inc.

K250469Accuro® 3S Needle Guide Kit K243937Accuro 3S

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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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