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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 the device name listed in this FDA 510(k) record. The listed applicant is Velox Manufacturing, Inc.. It received FDA 510(k) clearance on 2024-01-12 under 510(k) 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. The listed applicant is Velox Manufacturing, Inc.. The 510(k) number is K231315.

When did Velox Power Chair receive FDA 510(k) clearance?

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

Who is the listed applicant for Velox Power Chair?

The FDA 510(k) record lists Velox Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Velox Power Chair?

The FDA product code for Velox Power Chair is ITI.

Related Devices (Code: ITI)

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.

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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.

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