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FDA 510(k)

Y207 Electric Wheelchair

K-Number: K202482 · 2021-03-18

Decision Date2021-03-18
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Y207 Electric Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Intco Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2021-03-18 under 510(k) number K202482. 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 Y207 Electric Wheelchair?

Y207 Electric Wheelchair is a medical device that received FDA 510(k) clearance on 2021-03-18. The listed applicant is Jiangsu Intco Medical Products Co., Ltd.. The 510(k) number is K202482.

When did Y207 Electric Wheelchair receive FDA 510(k) clearance?

Y207 Electric Wheelchair received FDA 510(k) clearance on 2021-03-18, under 510(k) number K202482.

Who is the listed applicant for Y207 Electric Wheelchair?

The FDA 510(k) record lists Jiangsu Intco Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Y207 Electric Wheelchair?

The FDA product code for Y207 Electric Wheelchair is ITI.

Other records listing Jiangsu Intco Medical Products 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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