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FDA 510(k)

PERMOBIL POWERED WHEELCHAIR 1280

K-Number: K991658 · 1999-10-08

ApplicantPermobil AB
Decision Date1999-10-08
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERMOBIL POWERED WHEELCHAIR 1280 is the device name listed in this FDA 510(k) record. The listed applicant is Permobil AB. It received FDA 510(k) clearance on 1999-10-08 under 510(k) number K991658. 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 PERMOBIL POWERED WHEELCHAIR 1280?

PERMOBIL POWERED WHEELCHAIR 1280 is a medical device that received FDA 510(k) clearance on 1999-10-08. The listed applicant is Permobil AB. The 510(k) number is K991658.

When did PERMOBIL POWERED WHEELCHAIR 1280 receive FDA 510(k) clearance?

PERMOBIL POWERED WHEELCHAIR 1280 received FDA 510(k) clearance on 1999-10-08, under 510(k) number K991658.

Who is the listed applicant for PERMOBIL POWERED WHEELCHAIR 1280?

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

What is the FDA product code for PERMOBIL POWERED WHEELCHAIR 1280?

The FDA product code for PERMOBIL POWERED WHEELCHAIR 1280 is ITI.

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Other records listing Permobil AB 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.

K190682Explorer MiniK191874F5 Corpus VSK123290M300 & M400K103477PERMOBIL M300 / M400K081964K450 POWERED WHEELCHAIRK071650C350 POWERED 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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