GALAXY SERIES WHEELCHAIR
K-Number: K023993 · 2002-12-27
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Device Summary
Frequently Asked Questions
What is the GALAXY SERIES WHEELCHAIR?
GALAXY SERIES WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-12-27. The listed applicant is Evermed Corp.. The 510(k) number is K023993.
When did GALAXY SERIES WHEELCHAIR receive FDA 510(k) clearance?
GALAXY SERIES WHEELCHAIR received FDA 510(k) clearance on 2002-12-27, under 510(k) number K023993.
Who is the listed applicant for GALAXY SERIES WHEELCHAIR?
The FDA 510(k) record lists Evermed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GALAXY SERIES WHEELCHAIR?
The FDA product code for GALAXY SERIES 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 Evermed 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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