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FDA 510(k)

LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR

K-Number: K850876 · 1985-05-16

ApplicantKetronic, Inc.
Decision Date1985-05-16
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Ketronic, Inc.. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K850876. 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 LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR?

LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Ketronic, Inc.. The 510(k) number is K850876.

When did LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR receive FDA 510(k) clearance?

LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR received FDA 510(k) clearance on 1985-05-16, under 510(k) number K850876.

Who is the listed applicant for LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR?

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

What is the FDA product code for LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR?

The FDA product code for LIGTVOET L80.2 LIGHTFOOT L80.2 POWER WHEELCHAIR is ITI.

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Other records listing Ketronic, Inc. 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.

K850877MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFORK850869MFE COUCH ERGOMETERK850873HILO TABLES, TYPE CH-4, CH-8, FW-6, FW-5, FW-2, ALK850870MEDIFETTE ERGOMETERK850868MFE CARDIAC STRESS SYSTEMK850872PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI

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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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