YK9000 SERIES MANUAL WHEELCHAIR
K-Number: K052468 · 2005-10-05
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Device Summary
Frequently Asked Questions
What is the YK9000 SERIES MANUAL WHEELCHAIR?
YK9000 SERIES MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2005-10-05. The listed applicant is Intco Metal Products (Zhenjiang) Co., Ltd.. The 510(k) number is K052468.
When did YK9000 SERIES MANUAL WHEELCHAIR receive FDA 510(k) clearance?
YK9000 SERIES MANUAL WHEELCHAIR received FDA 510(k) clearance on 2005-10-05, under 510(k) number K052468.
Who is the listed applicant for YK9000 SERIES MANUAL WHEELCHAIR?
The FDA 510(k) record lists Intco Metal Products (Zhenjiang) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YK9000 SERIES MANUAL WHEELCHAIR?
The FDA product code for YK9000 SERIES MANUAL 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.
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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