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FDA 510(k)

DELUXE MANUAL WHEELCHAIR HW 4000

K-Number: K022700 · 2002-09-13

Decision Date2002-09-13
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DELUXE MANUAL WHEELCHAIR HW 4000 is the device name listed in this FDA 510(k) record. The listed applicant is Forever Young Ent. Co., Ltd.. It received FDA 510(k) clearance on 2002-09-13 under 510(k) number K022700. 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 DELUXE MANUAL WHEELCHAIR HW 4000?

DELUXE MANUAL WHEELCHAIR HW 4000 is a medical device that received FDA 510(k) clearance on 2002-09-13. The listed applicant is Forever Young Ent. Co., Ltd.. The 510(k) number is K022700.

When did DELUXE MANUAL WHEELCHAIR HW 4000 receive FDA 510(k) clearance?

DELUXE MANUAL WHEELCHAIR HW 4000 received FDA 510(k) clearance on 2002-09-13, under 510(k) number K022700.

Who is the listed applicant for DELUXE MANUAL WHEELCHAIR HW 4000?

The FDA 510(k) record lists Forever Young Ent. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELUXE MANUAL WHEELCHAIR HW 4000?

The FDA product code for DELUXE MANUAL WHEELCHAIR HW 4000 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 Forever Young Ent. 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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