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FDA 510(k)

GENEMAX POWER WHEELCHAIR, PW3

K-Number: K042748 · 2004-11-12

Decision Date2004-11-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GENEMAX POWER WHEELCHAIR, PW3 is the device name listed in this FDA 510(k) record. The listed applicant is Genemax Medical Products Industry Corp.. It received FDA 510(k) clearance on 2004-11-12 under 510(k) number K042748. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENEMAX POWER WHEELCHAIR, PW3?

GENEMAX POWER WHEELCHAIR, PW3 is a medical device that received FDA 510(k) clearance on 2004-11-12. The listed applicant is Genemax Medical Products Industry Corp.. The 510(k) number is K042748.

When did GENEMAX POWER WHEELCHAIR, PW3 receive FDA 510(k) clearance?

GENEMAX POWER WHEELCHAIR, PW3 received FDA 510(k) clearance on 2004-11-12, under 510(k) number K042748.

Who is the listed applicant for GENEMAX POWER WHEELCHAIR, PW3?

The FDA 510(k) record lists Genemax Medical Products Industry Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENEMAX POWER WHEELCHAIR, PW3?

The FDA product code for GENEMAX POWER WHEELCHAIR, PW3 is ITI.

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 Genemax Medical Products Industry Corp. 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: ITI)

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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