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FDA 510(k)

EXPLORER POWERED WHEELCHAIR

K-Number: K023485 · 2002-12-02

ApplicantEvermed Corp.
Decision Date2002-12-02
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXPLORER POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Evermed Corp.. It received FDA 510(k) clearance on 2002-12-02 under 510(k) number K023485. 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 EXPLORER POWERED WHEELCHAIR?

EXPLORER POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-12-02. The listed applicant is Evermed Corp.. The 510(k) number is K023485.

When did EXPLORER POWERED WHEELCHAIR receive FDA 510(k) clearance?

EXPLORER POWERED WHEELCHAIR received FDA 510(k) clearance on 2002-12-02, under 510(k) number K023485.

Who is the listed applicant for EXPLORER POWERED WHEELCHAIR?

The FDA 510(k) record lists Evermed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPLORER POWERED WHEELCHAIR?

The FDA product code for EXPLORER POWERED WHEELCHAIR 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 Evermed Corp. 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.

K023993GALAXY SERIES WHEELCHAIRK024030MILLENNIUM SERIES MANUAL WHEELCHAIRS

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

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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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