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FDA 510(k)

ELECTRIC MOBILITY'S SPARKY

K-Number: K874739 · 1988-04-22

ApplicantElectric Mobility, LLC
Decision Date1988-04-22
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRIC MOBILITY'S SPARKY is the device name listed in this FDA 510(k) record. The listed applicant is Electric Mobility, LLC. It received FDA 510(k) clearance on 1988-04-22 under 510(k) number K874739. 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 ELECTRIC MOBILITY'S SPARKY?

ELECTRIC MOBILITY'S SPARKY is a medical device that received FDA 510(k) clearance on 1988-04-22. The listed applicant is Electric Mobility, LLC. The 510(k) number is K874739.

When did ELECTRIC MOBILITY'S SPARKY receive FDA 510(k) clearance?

ELECTRIC MOBILITY'S SPARKY received FDA 510(k) clearance on 1988-04-22, under 510(k) number K874739.

Who is the listed applicant for ELECTRIC MOBILITY'S SPARKY?

The FDA 510(k) record lists Electric Mobility, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRIC MOBILITY'S SPARKY?

The FDA product code for ELECTRIC MOBILITY'S SPARKY is ITI.

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Other records listing Electric Mobility, LLC as applicant

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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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