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FDA 510(k)

Power Wheelchair (YH-E6011,YH-E6013A)

K-Number: K250134 · 2025-03-26

Decision Date2025-03-26
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Power Wheelchair (YH-E6011,YH-E6013A) is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Youhuan Automation Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-03-26 under 510(k) number K250134. 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 (YH-E6011,YH-E6013A)?

Power Wheelchair (YH-E6011,YH-E6013A) is a medical device that received FDA 510(k) clearance on 2025-03-26. The listed applicant is Ningbo Youhuan Automation Technology Co., Ltd.. The 510(k) number is K250134.

When did Power Wheelchair (YH-E6011,YH-E6013A) receive FDA 510(k) clearance?

Power Wheelchair (YH-E6011,YH-E6013A) received FDA 510(k) clearance on 2025-03-26, under 510(k) number K250134.

Who is the listed applicant for Power Wheelchair (YH-E6011,YH-E6013A)?

The FDA 510(k) record lists Ningbo Youhuan Automation Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Power Wheelchair (YH-E6011,YH-E6013A)?

The FDA product code for Power Wheelchair (YH-E6011,YH-E6013A) is ITI.

Other records listing Ningbo Youhuan Automation Technology Co., Ltd. as applicant

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.

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.

Official Source

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