CROSS SPORT, RIGID WHEELCHAIR
K-Number: K990358 · 1999-02-26
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Device Summary
Frequently Asked Questions
What is the CROSS SPORT, RIGID WHEELCHAIR?
CROSS SPORT, RIGID WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1999-02-26. The listed applicant is Tisport. The 510(k) number is K990358.
When did CROSS SPORT, RIGID WHEELCHAIR receive FDA 510(k) clearance?
CROSS SPORT, RIGID WHEELCHAIR received FDA 510(k) clearance on 1999-02-26, under 510(k) number K990358.
Who is the listed applicant for CROSS SPORT, RIGID WHEELCHAIR?
The FDA 510(k) record lists Tisport as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CROSS SPORT, RIGID WHEELCHAIR?
The FDA product code for CROSS SPORT, RIGID 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 Tisport 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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