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FDA 510(k)

Manual Wheelchair W54

K-Number: K180309 · 2019-05-03

Decision Date2019-05-03
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Manual Wheelchair W54 is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Jumao Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2019-05-03 under 510(k) number K180309. 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 W54?

Manual Wheelchair W54 is a medical device that received FDA 510(k) clearance on 2019-05-03. The listed applicant is Jiangsu Jumao Medical Equipment Co., Ltd.. The 510(k) number is K180309.

When did Manual Wheelchair W54 receive FDA 510(k) clearance?

Manual Wheelchair W54 received FDA 510(k) clearance on 2019-05-03, under 510(k) number K180309.

Who is the listed applicant for Manual Wheelchair W54?

The FDA 510(k) record lists Jiangsu Jumao Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Manual Wheelchair W54?

The FDA product code for Manual Wheelchair W54 is IOR.

Related Devices (Code: IOR)

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.

Official Source

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