MANUAL WHEELCHAIR SERIES
K-Number: K040561 · 2004-03-31
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Device Summary
Frequently Asked Questions
What is the MANUAL WHEELCHAIR SERIES?
MANUAL WHEELCHAIR SERIES is a medical device that received FDA 510(k) clearance on 2004-03-31. The listed applicant is Shanghai Wheelchair Factory. The 510(k) number is K040561.
When did MANUAL WHEELCHAIR SERIES receive FDA 510(k) clearance?
MANUAL WHEELCHAIR SERIES received FDA 510(k) clearance on 2004-03-31, under 510(k) number K040561.
Who is the listed applicant for MANUAL WHEELCHAIR SERIES?
The FDA 510(k) record lists Shanghai Wheelchair Factory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MANUAL WHEELCHAIR SERIES?
The FDA product code for MANUAL WHEELCHAIR SERIES 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.
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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