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FDA 510(k)

FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR

K-Number: K910753 · 1991-04-22

ApplicantFortress Litestyle
Decision Date1991-04-22
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Fortress Litestyle. It received FDA 510(k) clearance on 1991-04-22 under 510(k) number K910753. 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 FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR?

FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is Fortress Litestyle. The 510(k) number is K910753.

When did FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR receive FDA 510(k) clearance?

FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR received FDA 510(k) clearance on 1991-04-22, under 510(k) number K910753.

Who is the listed applicant for FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR?

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

What is the FDA product code for FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR?

The FDA product code for FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIR is ITI.

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Other records listing Fortress Litestyle 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.

K910751FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTERK910749FORTRESS MODEL 760-V 4 WHEEL POWER WHEELCHAIRK910747FORTRESS AEROEDGE 3-WHEEL MANUAL RACING WHEELCHAIRK910752FORTRESS LIBERTY MANUAL FOLDING WHEELCHAIRK910748FORTRESS EDGE MANUAL RIGID WHEELCHAIRK910746FORTRESS FREESTYLE II MANUAL FOLDING 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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