SKYWAY
K-Number: K964682 · 1997-01-13
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Device Summary
Frequently Asked Questions
What is the SKYWAY?
SKYWAY is a medical device that received FDA 510(k) clearance on 1997-01-13. The listed applicant is Kid'S Wheel-Chairs. The 510(k) number is K964682.
When did SKYWAY receive FDA 510(k) clearance?
SKYWAY received FDA 510(k) clearance on 1997-01-13, under 510(k) number K964682.
Who is the listed applicant for SKYWAY?
The FDA 510(k) record lists Kid'S Wheel-Chairs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SKYWAY?
The FDA product code for SKYWAY 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 Kid'S Wheel-Chairs 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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