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FDA 510(k)

Velox Power Chair

K-Number: K231315 · 2024-01-12

ApplicantVelox Manufacturing, Inc.
Decision Date2024-01-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Velox Power Chair is a medical device manufactured by Velox Manufacturing, Inc.. It received FDA 510(k) clearance on 2024-01-12 under approval number K231315. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Velox Power Chair?

Velox Power Chair is a medical device that received FDA 510(k) clearance on 2024-01-12. It is manufactured by Velox Manufacturing, Inc.. The 510(k) number is K231315.

When was Velox Power Chair approved by the FDA?

Velox Power Chair received FDA 510(k) clearance on 2024-01-12, under approval number K231315.

What company makes Velox Power Chair?

Velox Power Chair is manufactured by Velox Manufacturing, Inc..

What is the FDA product code for Velox Power Chair?

The FDA product code for Velox Power Chair is ITI.

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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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