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)

Electrically Powered Wheelchair, Joy Rider

K-Number: K220156 · 2022-10-07

Decision Date2022-10-07
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electrically Powered Wheelchair, Joy Rider is a medical device manufactured by Tung Keng Enterprise Co., Ltd.. It received FDA 510(k) clearance on 2022-10-07 under approval number K220156. 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 Electrically Powered Wheelchair, Joy Rider?

Electrically Powered Wheelchair, Joy Rider is a medical device that received FDA 510(k) clearance on 2022-10-07. It is manufactured by Tung Keng Enterprise Co., Ltd.. The 510(k) number is K220156.

When was Electrically Powered Wheelchair, Joy Rider approved by the FDA?

Electrically Powered Wheelchair, Joy Rider received FDA 510(k) clearance on 2022-10-07, under approval number K220156.

What company makes Electrically Powered Wheelchair, Joy Rider?

Electrically Powered Wheelchair, Joy Rider is manufactured by Tung Keng Enterprise Co., Ltd..

What is the FDA product code for Electrically Powered Wheelchair, Joy Rider?

The FDA product code for Electrically Powered Wheelchair, Joy Rider is ITI.

Related Clinical Trials

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.