KAIYANG STEEL WHEELCHAIR
K-Number: K101999 · 2010-10-04
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Device Summary
Frequently Asked Questions
What is the KAIYANG STEEL WHEELCHAIR?
KAIYANG STEEL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2010-10-04. The listed applicant is Guangdong Kaiyang Medical Technology Co., Ltd.. The 510(k) number is K101999.
When did KAIYANG STEEL WHEELCHAIR receive FDA 510(k) clearance?
KAIYANG STEEL WHEELCHAIR received FDA 510(k) clearance on 2010-10-04, under 510(k) number K101999.
Who is the listed applicant for KAIYANG STEEL WHEELCHAIR?
The FDA 510(k) record lists Guangdong Kaiyang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAIYANG STEEL WHEELCHAIR?
The FDA product code for KAIYANG STEEL 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 Guangdong Kaiyang Medical Technology Co., Ltd. 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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