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FDA 510(k)

JUMAO MANUAL WHEELCHAIR

K-Number: K082784 · 2008-10-07

Decision Date2008-10-07
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JUMAO MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Danyang Jumao Healthcare Equipment Co., Ltd.. It received FDA 510(k) clearance on 2008-10-07 under 510(k) number K082784. 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 JUMAO MANUAL WHEELCHAIR?

JUMAO MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2008-10-07. The listed applicant is Danyang Jumao Healthcare Equipment Co., Ltd.. The 510(k) number is K082784.

When did JUMAO MANUAL WHEELCHAIR receive FDA 510(k) clearance?

JUMAO MANUAL WHEELCHAIR received FDA 510(k) clearance on 2008-10-07, under 510(k) number K082784.

Who is the listed applicant for JUMAO MANUAL WHEELCHAIR?

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

What is the FDA product code for JUMAO MANUAL WHEELCHAIR?

The FDA product code for JUMAO MANUAL WHEELCHAIR is IOR.

Related Clinical Trials

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.

Other records listing Danyang Jumao Healthcare Equipment Co., Ltd. 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.

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

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