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FDA 510(k)

PRO WALKER PL-200 POWER WHEELCHAIR

K-Number: K041336 · 2004-07-20

ApplicantPro Walker, Inc.
Decision Date2004-07-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRO WALKER PL-200 POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Pro Walker, Inc.. It received FDA 510(k) clearance on 2004-07-20 under 510(k) number K041336. 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 PRO WALKER PL-200 POWER WHEELCHAIR?

PRO WALKER PL-200 POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2004-07-20. The listed applicant is Pro Walker, Inc.. The 510(k) number is K041336.

When did PRO WALKER PL-200 POWER WHEELCHAIR receive FDA 510(k) clearance?

PRO WALKER PL-200 POWER WHEELCHAIR received FDA 510(k) clearance on 2004-07-20, under 510(k) number K041336.

Who is the listed applicant for PRO WALKER PL-200 POWER WHEELCHAIR?

The FDA 510(k) record lists Pro Walker, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO WALKER PL-200 POWER WHEELCHAIR?

The FDA product code for PRO WALKER PL-200 POWER 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 Pro Walker, Inc. 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.

K041337PRO WALKER ML-300 FOLDABLE WHEELCHAIR

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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