Angiography Injector
K-Number: K242143 · 2024-12-23
Decision Date2024-12-23
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Angiography Injector is a medical device manufactured by Shandong Int Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2024-12-23 under approval 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. It is manufactured by Shandong Int Medical Instruments Co., Ltd.. The 510(k) number is K242143.
When was Angiography Injector approved by the FDA?
Angiography Injector received FDA 510(k) clearance on 2024-12-23, under approval number K242143.
What company makes Angiography Injector?
Angiography Injector is manufactured by Shandong Int Medical Instruments Co., Ltd..
What is the FDA product code for Angiography Injector?
The FDA product code for Angiography Injector is DXT.
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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.