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FDA 510(k)

Angiography Injector

K-Number: K242143 · 2024-12-23

Decision Date2024-12-23
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Angiography Injector is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Int Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K242143. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Angiography Injector?

Angiography Injector is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Shandong Int Medical Instruments Co., Ltd.. The 510(k) number is K242143.

When did Angiography Injector receive FDA 510(k) clearance?

Angiography Injector received FDA 510(k) clearance on 2024-12-23, under 510(k) number K242143.

Who is the listed applicant for Angiography Injector?

The FDA 510(k) record lists Shandong Int Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Angiography Injector?

The FDA product code for Angiography Injector is DXT.

Other records listing Shandong Int Medical Instruments 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: DXT)

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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