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FDA 510(k)

TEKNIQUE-HOVEROUND POWER WHEEL CHAIR

K-Number: K021136 · 2002-04-19

ApplicantHoveround Corp.
Decision Date2002-04-19
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TEKNIQUE-HOVEROUND POWER WHEEL CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Hoveround Corp.. It received FDA 510(k) clearance on 2002-04-19 under 510(k) number K021136. 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 TEKNIQUE-HOVEROUND POWER WHEEL CHAIR?

TEKNIQUE-HOVEROUND POWER WHEEL CHAIR is a medical device that received FDA 510(k) clearance on 2002-04-19. The listed applicant is Hoveround Corp.. The 510(k) number is K021136.

When did TEKNIQUE-HOVEROUND POWER WHEEL CHAIR receive FDA 510(k) clearance?

TEKNIQUE-HOVEROUND POWER WHEEL CHAIR received FDA 510(k) clearance on 2002-04-19, under 510(k) number K021136.

Who is the listed applicant for TEKNIQUE-HOVEROUND POWER WHEEL CHAIR?

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

What is the FDA product code for TEKNIQUE-HOVEROUND POWER WHEEL CHAIR?

The FDA product code for TEKNIQUE-HOVEROUND POWER WHEEL CHAIR is ITI.

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Other records listing Hoveround 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.

K122707HOVERROUND TEKNIQUEK122741HOVEROUND TEKNIQUEK100527HOVEROUND TEKNIQUE, MODEL HD-6K093946HOVEROUND HOVERGLIDE MODEL HOVERGLIDE MK-2K100350HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GTK090108HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR

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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.

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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