FDA 510(k)

UB 140

K-Number: K033827 · 2003-12-18

Decision Date2003-12-18

Product CodeITI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

UB 140 is the device name listed in this FDA 510(k) record. The listed applicant is Rivertrail Mobility. It received FDA 510(k) clearance on 2003-12-18 under 510(k) number K033827. 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 UB 140?

UB 140 is a medical device that received FDA 510(k) clearance on 2003-12-18. The listed applicant is Rivertrail Mobility. The 510(k) number is K033827.

When did UB 140 receive FDA 510(k) clearance?

UB 140 received FDA 510(k) clearance on 2003-12-18, under 510(k) number K033827.

Who is the listed applicant for UB 140?

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

What is the FDA product code for UB 140?

The FDA product code for UB 140 is ITI.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.