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FDA 510(k)

FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER

K-Number: K910751 · 1991-04-22

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

Device Summary

FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER 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 K910751. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER?

FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER 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 K910751.

When did FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER receive FDA 510(k) clearance?

FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER received FDA 510(k) clearance on 1991-04-22, under 510(k) number K910751.

Who is the listed applicant for FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER?

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 1600ACV REAR WHEEL DRIVE SCOOTER?

The FDA product code for FORTRESS 1600ACV REAR WHEEL DRIVE SCOOTER is INI.

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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.

K910753FORTRESS MODEL SPIRIT 4-WHEEL POWER WHEELCHAIRK910749FORTRESS 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: INI)

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.

K261078Electric Scooter (FNS01,FNS03)Anhui Jbh Medical Apparatus Co., Ltd.K261859Electric Scooter (FDB08, FDB08A, FDB12)Anhui JBH Medical Apparatus Co., Ltd.K260094Mobility Scooter (W3465, W3902 (S50 Carbon))Zhejiang Innuovo Rehabilitation Devices Co.,LtdK260176Mobility Scooter (W3483, W3483A)Zhejiang Innuovo Rehabilitation Devices Co.,LtdK261232IERO Mobility Scooter (IERO-01)Jochu Technology Co., Ltd.K261163Mobility Scooter (R200)Yongkang Ruihe Metal Product 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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