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FDA 510(k)

MULTIPLE, MODEL KTJ-50

K-Number: K043444 · 2005-02-22

Decision Date2005-02-22
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTIPLE, MODEL KTJ-50 is the device name listed in this FDA 510(k) record. The listed applicant is Golden Horse Medical Equipment (Wuxi) Co. , Ltd.. It received FDA 510(k) clearance on 2005-02-22 under 510(k) number K043444. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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