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 (N6101)

K-Number: K241686 · 2024-08-13

Decision Date2024-08-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Power wheelchair (N6101) is a medical device manufactured by Zhejiang Zhonglei Medical Technology Co. , Ltd.. It received FDA 510(k) clearance on 2024-08-13 under approval number K241686. 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 (N6101)?

Power wheelchair (N6101) is a medical device that received FDA 510(k) clearance on 2024-08-13. It is manufactured by Zhejiang Zhonglei Medical Technology Co. , Ltd.. The 510(k) number is K241686.

When was Power wheelchair (N6101) approved by the FDA?

Power wheelchair (N6101) received FDA 510(k) clearance on 2024-08-13, under approval number K241686.

What company makes Power wheelchair (N6101)?

Power wheelchair (N6101) is manufactured by Zhejiang Zhonglei Medical Technology Co. , Ltd..

What is the FDA product code for Power wheelchair (N6101)?

The FDA product code for Power wheelchair (N6101) is ITI.

Other Devices by Zhejiang Zhonglei Medical Technology Co. , Ltd.

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.