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FDA 510(k)

Electric Wheelchair [Models: JRWD6010/JRWD6012]

K-Number: K192739 · 2021-07-13

ApplicantJerry Medical Instrument (Shanghai) Co., Ltd.
Decision Date2021-07-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair [Models: JRWD6010/JRWD6012] is a medical device manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd.. It received FDA 510(k) clearance on 2021-07-13 under approval number K192739. 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 Electric Wheelchair [Models: JRWD6010/JRWD6012]?

Electric Wheelchair [Models: JRWD6010/JRWD6012] is a medical device that received FDA 510(k) clearance on 2021-07-13. It is manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd.. The 510(k) number is K192739.

When was Electric Wheelchair [Models: JRWD6010/JRWD6012] approved by the FDA?

Electric Wheelchair [Models: JRWD6010/JRWD6012] received FDA 510(k) clearance on 2021-07-13, under approval number K192739.

What company makes Electric Wheelchair [Models: JRWD6010/JRWD6012]?

Electric Wheelchair [Models: JRWD6010/JRWD6012] is manufactured by Jerry Medical Instrument (Shanghai) Co., Ltd..

What is the FDA product code for Electric Wheelchair [Models: JRWD6010/JRWD6012]?

The FDA product code for Electric Wheelchair [Models: JRWD6010/JRWD6012] is ITI.

Related Clinical Trials

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

K192658Manual Wheelchair

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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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