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FDA 510(k)

WU'S POWERED WHEELCHAIR, MAMBO 36X

K-Number: K050010 · 2005-02-11

Decision Date2005-02-11
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WU'S POWERED WHEELCHAIR, MAMBO 36X is the device name listed in this FDA 510(k) record. The listed applicant is Wu'S Tech Co., Ltd.. It received FDA 510(k) clearance on 2005-02-11 under 510(k) number K050010. 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 WU'S POWERED WHEELCHAIR, MAMBO 36X?

WU'S POWERED WHEELCHAIR, MAMBO 36X is a medical device that received FDA 510(k) clearance on 2005-02-11. The listed applicant is Wu'S Tech Co., Ltd.. The 510(k) number is K050010.

When did WU'S POWERED WHEELCHAIR, MAMBO 36X receive FDA 510(k) clearance?

WU'S POWERED WHEELCHAIR, MAMBO 36X received FDA 510(k) clearance on 2005-02-11, under 510(k) number K050010.

Who is the listed applicant for WU'S POWERED WHEELCHAIR, MAMBO 36X?

The FDA 510(k) record lists Wu'S Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WU'S POWERED WHEELCHAIR, MAMBO 36X?

The FDA product code for WU'S POWERED WHEELCHAIR, MAMBO 36X 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 Wu'S Tech 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.

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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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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