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FDA 510(k)

JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP

K-Number: K062218 · 2006-08-16

Decision Date2006-08-16
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP is the device name listed in this FDA 510(k) record. The listed applicant is Jan Mao Industries Co., Ltd.. It received FDA 510(k) clearance on 2006-08-16 under 510(k) number K062218. 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 JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP?

JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP is a medical device that received FDA 510(k) clearance on 2006-08-16. The listed applicant is Jan Mao Industries Co., Ltd.. The 510(k) number is K062218.

When did JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP receive FDA 510(k) clearance?

JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP received FDA 510(k) clearance on 2006-08-16, under 510(k) number K062218.

Who is the listed applicant for JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP?

The FDA 510(k) record lists Jan Mao Industries Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP?

The FDA product code for JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP 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 Jan Mao Industries 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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