MULTIPLE, MODEL KTJ-50
K-Number: K043444 · 2005-02-22
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Device Summary
Frequently Asked Questions
What is the MULTIPLE, MODEL KTJ-50?
MULTIPLE, MODEL KTJ-50 is a medical device that received FDA 510(k) clearance on 2005-02-22. The listed applicant is Golden Horse Medical Equipment (Wuxi) Co. , Ltd.. The 510(k) number is K043444.
When did MULTIPLE, MODEL KTJ-50 receive FDA 510(k) clearance?
MULTIPLE, MODEL KTJ-50 received FDA 510(k) clearance on 2005-02-22, under 510(k) number K043444.
Who is the listed applicant for MULTIPLE, MODEL KTJ-50?
The FDA 510(k) record lists Golden Horse Medical Equipment (Wuxi) Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIPLE, MODEL KTJ-50?
The FDA product code for MULTIPLE, MODEL KTJ-50 is DXQ.
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 Golden Horse Medical Equipment (Wuxi) 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: DXQ)
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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