Y.E.S POWERED WHEELCHAIR. T180
K-Number: K032512 · 2003-11-12
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Device Summary
Frequently Asked Questions
What is the Y.E.S POWERED WHEELCHAIR. T180?
Y.E.S POWERED WHEELCHAIR. T180 is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is Yeou Eir Shuen Machinery Co., Ltd.. The 510(k) number is K032512.
When did Y.E.S POWERED WHEELCHAIR. T180 receive FDA 510(k) clearance?
Y.E.S POWERED WHEELCHAIR. T180 received FDA 510(k) clearance on 2003-11-12, under 510(k) number K032512.
Who is the listed applicant for Y.E.S POWERED WHEELCHAIR. T180?
The FDA 510(k) record lists Yeou Eir Shuen Machinery Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Y.E.S POWERED WHEELCHAIR. T180?
The FDA product code for Y.E.S POWERED WHEELCHAIR. T180 is ITI.
Related Clinical Trials
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.
Other records listing Yeou Eir Shuen Machinery 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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