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FDA 510(k)

SUNPEX TECHNOLOGIES MODEL PW

K-Number: K024175 · 2003-05-01

ApplicantSunpex Technology Co., Ltd.
Decision Date2003-05-01
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUNPEX TECHNOLOGIES MODEL PW is the device name listed in this FDA 510(k) record. The listed applicant is Sunpex Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-05-01 under 510(k) number K024175. 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 SUNPEX TECHNOLOGIES MODEL PW?

SUNPEX TECHNOLOGIES MODEL PW is a medical device that received FDA 510(k) clearance on 2003-05-01. The listed applicant is Sunpex Technology Co., Ltd.. The 510(k) number is K024175.

When did SUNPEX TECHNOLOGIES MODEL PW receive FDA 510(k) clearance?

SUNPEX TECHNOLOGIES MODEL PW received FDA 510(k) clearance on 2003-05-01, under 510(k) number K024175.

Who is the listed applicant for SUNPEX TECHNOLOGIES MODEL PW?

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

What is the FDA product code for SUNPEX TECHNOLOGIES MODEL PW?

The FDA product code for SUNPEX TECHNOLOGIES MODEL PW 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.

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Other records listing Sunpex 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.

K033019SUNPEX TECHNOLOGIES MODEL SE03K021925SUNPEX TECHNOLOGIES MODEL SE 01K021371SUNSPEX TECHNOLOGIES MODEL SE 02

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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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