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FDA 510(k)

Y.E.S. POWERED WHEELCHAIR, MODEL T200

K-Number: K032669 · 2003-11-12

ApplicantYeou Eir Shuen Machinery Co., Ltd.
Decision Date2003-11-12
Product CodeITN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Y.E.S. POWERED WHEELCHAIR, MODEL T200 is the device name listed in this FDA 510(k) record. The listed applicant is Yeou Eir Shuen Machinery Co., Ltd.. It received FDA 510(k) clearance on 2003-11-12 under 510(k) number K032669. The device is classified under product code ITN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Y.E.S. POWERED WHEELCHAIR, MODEL T200?

Y.E.S. POWERED WHEELCHAIR, MODEL T200 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 K032669.

When did Y.E.S. POWERED WHEELCHAIR, MODEL T200 receive FDA 510(k) clearance?

Y.E.S. POWERED WHEELCHAIR, MODEL T200 received FDA 510(k) clearance on 2003-11-12, under 510(k) number K032669.

Who is the listed applicant for Y.E.S. POWERED WHEELCHAIR, MODEL T200?

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, MODEL T200?

The FDA product code for Y.E.S. POWERED WHEELCHAIR, MODEL T200 is ITN.

Related Clinical Trials

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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.

K032512Y.E.S POWERED WHEELCHAIR. T180

Related Devices (Code: ITN)

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.

K071028VIEWMATE SYSTEMEp MedsystemsK821256COUNTER-ROTATION SYSTEMThe Langer Group

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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