스텐트리언트 인젝터용 CT 시릴(스파이크, 프라임 튜브, 풀 튜브 포함 및 미포함), 스텐트리언트 인젝터용 CT 시릴 더블 팩(스파이크, 프라임 튜브, 풀 튜브 포함 및 미포함), 단일 패스와 램 튜브, 더블 패스와 램 튜브

CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), CT Syringe Dual Pack for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), Single Fascia and Ram Tip, Dual Fascia and Ram Tip is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is Coeur, Inc.. The 510(k) number is K170431.

CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), CT Syringe Dual Pack for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), Single Fascia and Ram Tip, Dual Fascia and Ram Tip received FDA 510(k) clearance on 2017-08-18, under 510(k) number K170431.

The FDA 510(k) record lists Coeur, Inc. as the applicant. This does not by itself establish the device manufacturer.

The FDA product code for CT Syringe for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), CT Syringe Dual Pack for Stellant Injectors (with & without Spikes, Prime Tubes, & Fill Tubes), Single Fascia and Ram Tip, Dual Fascia and Ram Tip is DXT.