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FDA 510(k)

Manual Wheelchair

K-Number: K192658 · 2020-04-01

ApplicantJerry Medical Instrument (Shanghai) Co., Ltd.
Decision Date2020-04-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Manual Wheelchair is a medical device manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd.. It received FDA 510(k) clearance on 2020-04-01 under approval number K192658. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Manual Wheelchair?

Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2020-04-01. It is manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd.. The 510(k) number is K192658.

When was Manual Wheelchair approved by the FDA?

Manual Wheelchair received FDA 510(k) clearance on 2020-04-01, under approval number K192658.

What company makes Manual Wheelchair?

Manual Wheelchair is manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd..

What is the FDA product code for Manual Wheelchair?

The FDA product code for Manual Wheelchair is IOR.

Related Clinical Trials

NCT05776030 Multi-speed Ergonomic Wheelchair RECRUITING NCT04668326 Mobile Manual Standing Wheelchair for SCI COMPLETED

Other Devices by Jerry Medical Instrument (Shanghai) Co., Ltd.

K192739Electric Wheelchair [Models: JRWD6010/JRWD6012]

Related Devices (Code: IOR)

K162696Kuschall Advance Manual WheelchairInvacare Corporation K162686Kuschall Champion Manual WheelchairInvacare Corporation K162692Kuschall K-Series Attract Manual WheelchairInvacare Corporation K161425APEX Manual WheelchairMotion Composites K153328SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd. K151492KuduR82 A/S

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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