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FDA 510(k)

EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR

K-Number: K002671 · 2000-10-11

Decision Date2000-10-11
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Intco Medical Equipment & Supply Co., Ltd.. It received FDA 510(k) clearance on 2000-10-11 under 510(k) number K002671. 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 EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR?

EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2000-10-11. The listed applicant is Jiangsu Intco Medical Equipment & Supply Co., Ltd.. The 510(k) number is K002671.

When did EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR receive FDA 510(k) clearance?

EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR received FDA 510(k) clearance on 2000-10-11, under 510(k) number K002671.

Who is the listed applicant for EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR?

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

What is the FDA product code for EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR?

The FDA product code for EZ-TRAVELER 2500 SERIES 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 Jiangsu Intco Medical Equipment & Supply 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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