Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Power Wheelchair

K-Number: K221026 · 2022-07-01

Decision Date2022-07-01
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Power Wheelchair is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2022-07-01 under approval number K221026. 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 Power Wheelchair?

Power Wheelchair is a medical device that received FDA 510(k) clearance on 2022-07-01. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K221026.

When was Power Wheelchair approved by the FDA?

Power Wheelchair received FDA 510(k) clearance on 2022-07-01, under approval number K221026.

What company makes Power Wheelchair?

Power Wheelchair is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.

What is the FDA product code for Power Wheelchair?

The FDA product code for Power Wheelchair is ITI.

Other Devices by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd

View all 16 devices →

Related Devices (Code: ITI)

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.